Diazepam
- Product NDC
- 72189-570
- 11-digit product format
- 721890570
- Labeler code
- 72189
- Product ID
- 72189-570_2047f721-6a06-c391-e063-6394a90a4ed7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_rx
- Application
- ANDA070325
- Marketing category
- ANDA
- Marketing start
- 2024-08-22
- Substance
- DIAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Q3JTX2Q7TU | DIAZEPAM | 439-14-5 | DIAZEPAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-570-30 | 72189057030 | 30 TABLET in 1 BOTTLE, PLASTIC (72189-570-30) | 30 tablet | 2024-08-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Diazepam | Direct_rx | 2024-08-22 | HUMAN PRESCRIPTION DRUG LABEL | 1 |