Diazepam
- Product NDC
- 35356-812
- 11-digit product format
- 353560812
- Labeler code
- 35356
- Product ID
- 35356-812_b8f7196d-8813-4320-80d9-21ee7530f954
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA071322
- Marketing category
- ANDA
- Marketing start
- 2010-12-31
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35356-812-60 | 35356081260 | 60 TABLET in 1 BOTTLE (35356-812-60) | 60 tablet | 2020-10-07 | 0000-00-00 | No | No | Current |
| 35356-812-90 | 35356081290 | 90 TABLET in 1 BOTTLE (35356-812-90) | 90 tablet | 2020-05-15 | 0000-00-00 | No | No | Current |