321bupe321
Greenlighter
- Joined
- Oct 10, 2016
- Messages
- 3
Well I just came across something extremely interesting, you'll think so too if on suboxone. Ive been on it in the past, the old stop sign 8/2's. I just got back on the strips a month ago and have been going insane as they have barely been having any effect whatsoever. I've been swearing up and down something was wrong with these strips as I pay big bucks for the visits and scripts. Even filed a cimplaint with the FDA. Well today an NDC code search gave a hell of a revelation.
Suboxone strips, despite what theyre labeled actually come as follows (and Dr.s & pharmacists probably won't like this but who are they to lie to patients in my book).
If the 4 different labeled strength, each actually comes as 2 strengths. Oh and the naloxone, only comes as 1mg in EVERY STRIP weather it matters or not. Each of the 4 *labeled strengths with their 2 different potential dosages have the same exact labeling and packaging including NDC code.
The 2/0.5 actually come as either 2/1 or 0.5/1. The 4/1 actually come as 4/1 or1/1. The 8/2 actually come as 8/1 or 2/1. The 12/3 that i was just raised to because the 2/1's i was getting and being told were 8/2 werent doing anything and still in withdrawal,actually come as 12/1 or 3/1. The latter of which I'm getting now being told its 12/3 as my asshole Dr fetd irritated when I tell him its nit working. Here's the source:
12496-1202-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 2 mg/1, .5 mg/1
NDC Package Code: 12496-1202-3
Product NDC: 12496-1202
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 09-13-2010
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1202-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1202-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII
12496-1204-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 4 mg/1, 1 mg/1
NDC Package Code: 12496-1204-3
Product NDC: 12496-1204
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 08-24-2012
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1204-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1204-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
12496-1208-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 8 mg/1, 2 mg/1
NDC Package Code: 12496-1208-3
Product NDC: 12496-1208
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 09-13-2010
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1208-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1208-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII
12496-1212-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 12 mg/1, 3 mg/1
NDC Package Code: 12496-1212-3
Product NDC: 12496-1212
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 08-24-2012
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1212-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII
12496-1212-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 12 mg/1, 3 mg/1
NDC Package Code: 12496-1212-3
Product NDC: 12496-1212
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 08-24-2012
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1212-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII.
http://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm
Suboxone strips, despite what theyre labeled actually come as follows (and Dr.s & pharmacists probably won't like this but who are they to lie to patients in my book).
If the 4 different labeled strength, each actually comes as 2 strengths. Oh and the naloxone, only comes as 1mg in EVERY STRIP weather it matters or not. Each of the 4 *labeled strengths with their 2 different potential dosages have the same exact labeling and packaging including NDC code.
The 2/0.5 actually come as either 2/1 or 0.5/1. The 4/1 actually come as 4/1 or1/1. The 8/2 actually come as 8/1 or 2/1. The 12/3 that i was just raised to because the 2/1's i was getting and being told were 8/2 werent doing anything and still in withdrawal,actually come as 12/1 or 3/1. The latter of which I'm getting now being told its 12/3 as my asshole Dr fetd irritated when I tell him its nit working. Here's the source:
12496-1202-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 2 mg/1, .5 mg/1
NDC Package Code: 12496-1202-3
Product NDC: 12496-1202
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 09-13-2010
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1202-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1202-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII
12496-1204-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 4 mg/1, 1 mg/1
NDC Package Code: 12496-1204-3
Product NDC: 12496-1204
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 08-24-2012
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1204-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1204-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
12496-1208-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 8 mg/1, 2 mg/1
NDC Package Code: 12496-1208-3
Product NDC: 12496-1208
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 09-13-2010
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1208-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1208-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII
12496-1212-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 12 mg/1, 3 mg/1
NDC Package Code: 12496-1212-3
Product NDC: 12496-1212
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 08-24-2012
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1212-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII
12496-1212-3 | Suboxone | buprenorphine hydrochloride, naloxone hydrochloride | FILM, SOLUBLE | 12 mg/1, 3 mg/1
NDC Package Code: 12496-1212-3
Product NDC: 12496-1212
Labeler Name: Indivior Inc.
Proprietary Name: Suboxone
Nonproprietary Name: buprenorphine hydrochloride, naloxone hydrochloride
Substance Name: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Product Type Name: HUMAN PRESCRIPTION DRUG
Start Marketing Date: 08-24-2012
End Marketing Date: N/A
Market Category: NDA
Application Number: NDA022410
Package Description: 30 POUCH in 1 CARTON (12496-1212-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1)
Pharm Class: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA: CIII.
http://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm