0228-3156 : Buprenorphine 2 mg Sublingual Tablet

NDC:	0228-3156
Labeler:	Actavis Pharma, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Buprenorphine
Dosage Form:	Sublingual Tablet
Application #:	ANDA090819
Rev. Date:	Apr 10, 2015
CSA Schedule:	CIII (US) ^[1]

^[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	156
Shapes:	Oval
Colors:	Orange
Size (mm):	9
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

0228-3156-03: 30 TABLET IN 1 BOTTLE (0228‑3156‑03)
0228-3156-09: 90 TABLET IN 1 BOTTLE (0228‑3156‑09)
0228-3156-73: 30 TABLET IN 1 BLISTER PACK (0228‑3156‑73)

Active Ingredients:

Buprenorphine Hydrochloride

Dosage Strength:

2 mg

Inactive Ingredients:

Anhydrous Citric Acid
Crospovidone
Fd&c Yellow No. 6
Lactose Monohydrate
Magnesium Stearate
Mannitol
Starch, Corn
Povidones
Trisodium Citrate Dihydrate

Pharmaceutical Classes:

Partial Opioid Agonist [EPC]
Partial Opioid Agonists [MoA]

NDC QR Code

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NDC 0228-3156 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.