Valium
- Product NDC
- 80725-006
- 11-digit product format
- 807250006
- Labeler code
- 80725
- Product ID
- 80725-006_ecf958a2-2749-5198-e053-2995a90a4def
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Waylis Therapuetics LLC
- Application
- NDA013263
- Marketing category
- NDA
- Marketing start
- 2022-04-04
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 10 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80725-006-01 | Valium | 100 in 1 BOTTLE | TABLET | 100 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80725-006 | VALIUM (DIAZEPAM) TABLET [WAYLIS THERAPUETICS LLC] | 9 | Legacy NDC, 1 package rows | 20241116_260e2041-2bb3-482f-850e-b5d47a7bdbe6.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 |
|---|
| 80725-006-01 | 80725000601 | 100 TABLET in 1 BOTTLE (80725-006-01) | 100 tablet | 2022-04-04 | 0000-00-00 | No | No | Current |