50090-5095 : Zolpidem Tartrate 10 mg Oral Tablet, Film Coated

NDC:	50090-5095
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Zolpidem Tartrate
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA078413
Rev. Date:	May 4, 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:	E;79
Shapes:	Oval
Colors:	White
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:

50090-5095-0: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑5095‑0)

Active Ingredients:

Zolpidem Tartrate

Dosage Strength:

10 mg

Inactive Ingredients:

Lactose Monohydrate
Microcrystalline Cellulose
Sodium Starch Glycolate Type a Potato
Magnesium Stearate
Hypromellose 2910 (5 Mpa.s)
Polyethylene Glycol 400
Titanium Dioxide /

Pharmaceutical Classes:

Central Nervous System Depression [PE]
GABA A Agonists [MoA]
Pyridines [CS]
gamma-Aminobutyric Acid-ergic Agonist [EPC]

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.