Diazepam
- Product NDC
- 21695-263
- 11-digit product format
- 216950263
- Labeler code
- 21695
- Product ID
- 21695-263_2d96a6cb-326f-4c04-b5d7-24d7f7c20699
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA071307
- Marketing category
- ANDA
- Marketing start
- 2009-11-09
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- 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 |
|---|
| 21695-263-30 | Diazepam | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 21695-263-90 | Diazepam | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-263 | DIAZEPAM TABLET [REBEL DISTRIBUTORS CORP.] | 1 | Legacy NDC, 2 package rows | 20100921_2d96a6cb-326f-4c04-b5d7-24d7f7c20699.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-263-30 | 21695026330 | 30 in 1 BOTTLE | Historical |
| 21695-263-90 | 21695026390 | 90 in 1 BOTTLE | Historical |