Diazepam
- Product NDC
- 68071-3330
- 11-digit product format
- 680713330
- Labeler code
- 68071
- Product ID
- 68071-3330_bb2b4c9e-7db1-c0be-e053-2a95a90aa2db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3330-1 | 68071333001 | 10 TABLET in 1 BOTTLE (68071-3330-1) | 10 tablet | 2017-07-11 | 0000-00-00 | No | No | Current |
| 68071-3330-3 | 68071333003 | 30 TABLET in 1 BOTTLE (68071-3330-3) | 30 tablet | 2017-07-11 | 0000-00-00 | No | No | Current |
| 68071-3330-5 | 68071333005 | 15 TABLET in 1 BOTTLE (68071-3330-5) | 15 tablet | 2017-07-11 | 0000-00-00 | No | No | Current |
| 68071-3330-6 | 68071333006 | 60 TABLET in 1 BOTTLE (68071-3330-6) | 60 tablet | 2017-07-11 | 0000-00-00 | No | No | Current |
| 68071-3330-9 | 68071333009 | 90 TABLET in 1 BOTTLE (68071-3330-9) | 90 tablet | 2017-07-11 | 0000-00-00 | No | No | Current |