Triazolam
- Product NDC
- 55289-787
- 11-digit product format
- 552890787
- Labeler code
- 55289
- Product ID
- 55289-787_dd0471dc-c829-eecd-e053-2995a90aab12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA017892
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1982-11-15
- 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 |
|---|
| 55289-787-02 | 55289078702 | 2 TABLET in 1 BOTTLE, PLASTIC (55289-787-02) | 2 tablet | 2010-01-12 | 0000-00-00 | No | No | Current |
| 55289-787-30 | 55289078730 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-787-30) | 30 tablet | 2010-05-25 | 0000-00-00 | No | No | Current |
| 55289-787-60 | 55289078760 | 60 TABLET in 1 BOTTLE, PLASTIC (55289-787-60) | 60 tablet | 2010-10-18 | 0000-00-00 | No | No | Current |