temazepam
- Product NDC
- 71335-2302
- 11-digit product format
- 713352302
- Labeler code
- 71335
- Product ID
- 71335-2302_de9cf2dc-75c3-4333-954f-e5682094c588
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- temazepam
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071457
- Marketing category
- ANDA
- Marketing start
- 1987-04-21
- Substance
- TEMAZEPAM
- Active strength
- 30 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 |
|---|
| CHB1QD2QSS | TEMAZEPAM | 846-50-4 | TEMAZEPAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2302-1 | 71335230201 | 500 CAPSULE in 1 BOTTLE (71335-2302-1) | 500 capsule | 2023-12-01 | No | No | Historical |