Zolpidem Tartrate
- Product NDC
- 61442-231
- 11-digit product format
- 614420231
- Labeler code
- 61442
- Product ID
- 61442-231_14e44cf8-d4c1-5424-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carlsbad Technology, Inc.
- Application
- ANDA077990
- Marketing category
- ANDA
- Marketing start
- 2007-04-23
- Marketing end
- 0000-00-00
- Substance
- ZOLPIDEM TARTRATE
- Active strength
- 5 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
FDA-Initiated Inactive NDC Indexing#