Zolpidem
- Product NDC
- 70934-917
- 11-digit product format
- 709340917
- Labeler code
- 70934
- Product ID
- 70934-917_d04d19c0-dfb3-7eef-e053-2a95a90a0dd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA077214
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- 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
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-917-30 | 70934091730 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-917-30) | 30 tablet | 2021-11-01 | 0000-00-00 | No | No | Current |