Diazepam
- Product NDC
- 60760-934
- 11-digit product format
- 607600934
- Labeler code
- 60760
- Product ID
- 60760-934_7b204c01-2d34-219c-e053-2991aa0a4b22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2018-07-30
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 60760-934-30 | 60760093430 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-934-30) | 30 tablet | 2018-07-30 | 0000-00-00 | No | No | Current |