Diazepam
- Product NDC
- 0527-1768
- 11-digit product format
- 005271768
- Labeler code
- 0527
- Product ID
- 0527-1768_4e8bea06-e0cc-4c92-a591-d1970c659d6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA204433
- Marketing category
- ANDA
- Marketing start
- 2014-04-14
- Marketing end
- 2023-08-31
- Substance
- DIAZEPAM
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0527-1768-36 | 00527176836 | 1 BOTTLE, DROPPER in 1 CARTON (0527-1768-36) > 30 mL in 1 BOTTLE, DROPPER | 2014-04-14 | 0000-00-00 | No | No | Current |