Zolpidem Tartrate Extended Release
- Product NDC
- 60760-116
- 11-digit product format
- 607600116
- Labeler code
- 60760
- Product ID
- 60760-116_77e68d0b-c9f6-b796-e053-2991aa0a3918
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ZOLPIDEM TARTRATE
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA078148
- Marketing category
- ANDA
- Marketing start
- 2013-01-10
- Marketing end
- 2019-06-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record