Temazepam
- Product NDC
- 70518-2926
- 11-digit product format
- 705182926
- Labeler code
- 70518
- Product ID
- 70518-2926_d4242af2-7c99-a4aa-e053-2995a90ad2af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Temazepam
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071620
- Marketing category
- ANDA
- Marketing start
- 2020-10-29
- Marketing end
- 0000-00-00
- Substance
- TEMAZEPAM
- Active strength
- 30 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 |
|---|
| 70518-2926-0 | 70518292600 | 100 POUCH in 1 BOX (70518-2926-0) > 1 CAPSULE in 1 POUCH (70518-2926-1) | 100 pouch | 2020-10-29 | 0000-00-00 | No | No | Current |