Zolpidem Tartrate
- Product NDC
- 67296-0759
- 11-digit product format
- 672960759
- Labeler code
- 67296
- Product ID
- 67296-0759_2ac71f36-5d44-41fd-b850-d3c20d968623
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA078616
- Marketing category
- ANDA
- Marketing start
- 2008-11-21
- 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]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-0759-1 | Zolpidem Tartrate | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0759 | ZOLPIDEM TARTRATE (ZOLPIDEM TARTRATE) TABLET [REDPHARM DRUG INC.] | 1 | Legacy NDC, 1 package rows | 20110808_a4de4fbc-56d2-40ac-814e-0546bca5ca7c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0759-1 | 67296075901 | 30 in 1 BOTTLE | Historical |