Zolpidem tartrate
- Product NDC
- 50436-3031
- 11-digit product format
- 504363031
- Labeler code
- 50436
- Product ID
- 50436-3031_e62c15ca-46f0-4750-b155-f1b8014dc849
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem tartrate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA090107
- Marketing category
- ANDA
- Marketing start
- 2011-10-31
- Marketing end
- 0000-00-00
- Substance
- ZOLPIDEM TARTRATE
- Active strength
- 13 mg/1
- Pharmacologic classes
- gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [CS],Central Nervous System Depression [PE]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record