Valium
- Product NDC
- 72189-401
- 11-digit product format
- 721890401
- Labeler code
- 72189
- Product ID
- 72189-401_efdf321a-5386-b897-e053-2995a90a7ee6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2022-12-05
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72189-401-02 | Diazepam | 2 in 1 BOTTLE | TABLET | 2 | | 5 |
| 72189-401-30 | Diazepam | 30 in 1 BOTTLE | TABLET | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-401 | DIAZEPAM TABLET [DIRECT_RX] | 5 | Legacy NDC, 2 package rows | 20230309_ef1a2b14-13ee-5d01-e053-2995a90a48c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-401-02 | 72189040102 | 2 TABLET in 1 BOTTLE (72189-401-02) | 2 tablet | 2022-12-05 | 0000-00-00 | No | No | Current |
| 72189-401-30 | 72189040130 | 30 TABLET in 1 BOTTLE (72189-401-30) | 30 tablet | 2022-12-05 | 0000-00-00 | No | No | Current |