DIAZEPAM
- Product NDC
- 59651-652
- 11-digit product format
- 596510652
- Labeler code
- 59651
- Product ID
- 59651-652_2f799120-0d08-47cd-8183-a98f0267c845
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIAZEPAM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA217843
- Marketing category
- ANDA
- Marketing start
- 2023-12-14
- Substance
- DIAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DIAZEPAM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIAZEPAM | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q3JTX2Q7TU |
| Rxcui | 197589, 197590, 197591 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59651-652-01 | DIAZEPAM | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 59651-652-05 | DIAZEPAM | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59651-652 | DIAZEPAM TABLET [AUROBINDO PHARMA LIMITED] | 1 | Current NDC, 2 package rows | 20231219_2f799120-0d08-47cd-8183-a98f0267c845.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59651-652-01 | 59651065201 | 100 TABLET in 1 BOTTLE (59651-652-01) | 100 tablet | 2023-12-14 | No | No | Current |
| 59651-652-05 | 59651065205 | 500 TABLET in 1 BOTTLE (59651-652-05) | 500 tablet | 2023-12-14 | No | No | Current |