Zolpidem Tartrate
- Product NDC
- 71335-1801
- 11-digit product format
- 713351801
- Labeler code
- 71335
- Product ID
- 71335-1801_daec339f-26f9-42b5-b8b4-3102bb8b7425
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078148
- Marketing category
- ANDA
- Marketing start
- 2011-04-14
- Marketing end
- 2023-06-30
- Substance
- ZOLPIDEM TARTRATE
- Active strength
- 6 mg/1
- Pharmacologic classes
- Central Nervous System Depression [PE], GABA A Agonists [MoA], Pyridines [CS], gamma-Aminobutyric Acid-ergic Agonist [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 71335-1801-1 | 71335180101 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1801-1) | 2021-12-20 | 0000-00-00 | No | No | Current |
| 71335-1801-2 | 71335180102 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1801-2) | 2021-12-20 | 0000-00-00 | No | No | Current |
| 71335-1801-3 | 71335180103 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1801-3) | 2021-12-20 | 0000-00-00 | No | No | Current |
| 71335-1801-4 | 71335180104 | 8 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1801-4) | 2021-12-20 | 0000-00-00 | No | No | Current |