temazepam
- Product NDC
- 63739-877
- 11-digit product format
- 637390877
- Labeler code
- 63739
- Product ID
- 63739-877_b3eb7633-2be2-dad1-e053-2995a90a70ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- temazepam
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA071456
- Marketing category
- ANDA
- Marketing start
- 1987-04-21
- Marketing end
- 0000-00-00
- Substance
- TEMAZEPAM
- Active strength
- 15 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63739-877-10 | 63739087710 | 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-877-10) > 10 CAPSULE in 1 BLISTER PACK | 3 blister pack | 2017-06-01 | 0000-00-00 | No | No | Current |