0115-8333 : Alprazolam 2 mg 24 Hr Extended Release Tablet

NDC:	0115-8333
Labeler:	Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type:	Human Prescription Drug
Drug Name:	Alprazolam
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA077968
Rev. Date:	May 24, 2007
CSA Schedule:	CIV (US) ^[1]

^[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	833
Shapes:	Round
Colors:	Blue
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:

0115-8333-02: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE (0115‑8333‑02)
0115-8333-13: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (0115‑8333‑13)

Active Ingredients:

Alprazolam

Dosage Strength:

2 mg

Inactive Ingredients:

Hypromellose
Lactose Monohydrate
Silicon Dioxide
Magnesium Stearate
Fd&c Blue No. 2

Pharmaceutical Classes:

Benzodiazepine [EPC]
Benzodiazepines [Chemical/Ingredient]

NDC 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.