Valium
- Product NDC
- 0140-0006
- 11-digit product format
- 001400006
- Labeler code
- 0140
- Product ID
- 0140-0006_5da13043-2476-406e-8658-834dfdb39530
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Roche Laboratories Inc.
- Application
- NDA013263
- Marketing category
- NDA
- Marketing start
- 1963-11-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0140-0006-01 | 00140000601 | 1 BOTTLE, PLASTIC in 1 CARTON (0140-0006-01) > 100 TABLET in 1 BOTTLE, PLASTIC | 1963-11-15 | 0000-00-00 | No | No | Current |
| 0140-0006-14 | 00140000614 | 1 BOTTLE, PLASTIC in 1 CARTON (0140-0006-14) > 500 TABLET in 1 BOTTLE, PLASTIC | 1963-11-15 | 0000-00-00 | No | No | Current |