Triazolam
- Product NDC
- 43063-996
- 11-digit product format
- 430630996
- Labeler code
- 43063
- Product ID
- 43063-996_e3b3fc13-18b8-6017-e053-2995a90a314d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA074224
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- Marketing end
- 0000-00-00
- Substance
- TRIAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-996-02 | 43063099602 | 2 TABLET in 1 BOTTLE, PLASTIC (43063-996-02) | 2 tablet | 2019-12-17 | 0000-00-00 | No | No | Current |
| 43063-996-30 | 43063099630 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-996-30) | 30 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |