Temazepam
- Product NDC
- 70518-3093
- 11-digit product format
- 705183093
- Labeler code
- 70518
- Product ID
- 70518-3093_c238729d-a785-4155-e053-2995a90aade5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Temazepam
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211542
- Marketing category
- ANDA
- Marketing start
- 2021-05-11
- Marketing end
- 0000-00-00
- Substance
- TEMAZEPAM
- Active strength
- 23 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 |
|---|
| 70518-3093-0 | 70518309300 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3093-0) | 30 capsule | 2021-05-11 | 0000-00-00 | No | No | Current |