Zolpidem Tartrate
- Product NDC
- 51407-554
- 11-digit product format
- 514070554
- Labeler code
- 51407
- Product ID
- 51407-554_ab83e3c3-e78c-2daf-e053-2995a90aa714
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA078148
- Marketing category
- ANDA
- Marketing start
- 2011-04-14
- Marketing end
- 0000-00-00
- Substance
- ZOLPIDEM TARTRATE
- Active strength
- 6 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-554-01 | 51407055401 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51407-554-01) | 2020-04-17 | 0000-00-00 | No | No | Current |