Zolpidem Tartrate
- Product NDC
- 55154-5080
- 11-digit product format
- 551545080
- Labeler code
- 55154
- Product ID
- 55154-5080_ee68d2b8-b8d5-44c2-898c-fa8f5af9e310
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zolpidem tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076578
- Marketing category
- ANDA
- Marketing start
- 2011-01-28
- Marketing end
- 0000-00-00
- Substance
- ZOLPIDEM TARTRATE
- Active strength
- 10 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record