Diazepam
- Product NDC
- 0093-6139
- 11-digit product format
- 000936139
- Labeler code
- 0093
- Product ID
- 0093-6139_4d523136-2ec4-4d85-9faf-801d75e24819
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- GEL
- Route
- RECTAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- NDA020648
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2010-09-03
- Marketing end
- 2021-09-30
- Substance
- DIAZEPAM
- Active strength
- 20 mg/4mL
- 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 |
|---|
| 0093-6139-32 | 00093613932 | 2 SYRINGE, PLASTIC in 1 PACKAGE (0093-6139-32) > 4 mL in 1 SYRINGE, PLASTIC | 2010-09-03 | 2021-09-30 | No | No | Current |