Diazepam
- Product NDC
- 55700-058
- 11-digit product format
- 557000058
- Labeler code
- 55700
- Product ID
- 55700-058_f82af446-40fe-47bf-8090-e0c6039b4440
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA071307
- Marketing category
- ANDA
- Marketing start
- 2018-07-13
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 2 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-058-30 | 55700005830 | 30 TABLET in 1 BOTTLE (55700-058-30) | 30 tablet | 2018-07-13 | 0000-00-00 | No | No | Current |
| 55700-058-90 | 55700005890 | 90 TABLET in 1 BOTTLE (55700-058-90) | 90 tablet | 2020-10-26 | 0000-00-00 | No | No | Current |