Zaleplon
- Product NDC
- 50436-1006
- 11-digit product format
- 504361006
- Labeler code
- 50436
- Product ID
- 50436-1006_e85ee5db-46e6-4b44-a456-3fcb5b8bc0fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zaleplon
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077239
- Marketing category
- ANDA
- Marketing start
- 2008-06-06
- Marketing end
- 0000-00-00
- Substance
- ZALEPLON
- Active strength
- 10 mg/1
- Pharmacologic classes
- gamma-Aminobutyric Acid A Receptor Agonist [EPC],GABA A Agonists [MoA],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