Zolpidem Tartrate
- Product NDC
- 0615-8046
- 11-digit product format
- 006158046
- Labeler code
- 0615
- Product ID
- 0615-8046_13706bb3-1f82-4581-b11b-8de8a4d6d93f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076410
- Marketing category
- ANDA
- Marketing start
- 2007-04-23
- Marketing end
- 2020-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record