Zolpidem Tartrate
- Product NDC
- 0615-8226
- 11-digit product format
- 006158226
- Labeler code
- 0615
- Product ID
- 0615-8226_80b88732-7b18-4d2c-a564-7e194a0cfcf4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA078413
- Marketing category
- ANDA
- Marketing start
- 2018-10-02
- Marketing end
- 2023-09-30
- 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
- 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 |
|---|
| 0615-8226-39 | 00615822639 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8226-39) | 2018-10-02 | 2023-09-30 | No | No | Current |