DIAZEPAM
- Product NDC
- 72189-193
- 11-digit product format
- 721890193
- Labeler code
- 72189
- Product ID
- 72189-193_cd0ee3a5-d1e4-540c-e053-2995a90a6aaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIAZEPAM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA071307
- Marketing category
- ANDA
- Marketing start
- 2021-08-24
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 72189-193-30 | DIAZEPAM | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-193 | DIAZEPAM TABLET [DIRECTRX] | 2 | Legacy NDC, 1 package rows | 20211016_ca4e3709-85c1-1dfe-e053-2a95a90a4be3.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 |
|---|
| 72189-193-30 | 72189019330 | 30 TABLET in 1 BOTTLE (72189-193-30) | 30 tablet | 2021-08-24 | 0000-00-00 | No | No | Current |