Flurazepam Hydrochloride
- Product NDC
- 55289-038
- 11-digit product format
- 552890038
- Labeler code
- 55289
- Product ID
- 55289-038_d83f043c-5be1-74fb-e053-2a95a90ab5e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- flurazepam hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA070345
- Marketing category
- ANDA
- Marketing start
- 1985-11-27
- Marketing end
- 2023-01-31
- Substance
- FLURAZEPAM HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 55289-038-30 | 55289003830 | 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-038-30) | 30 capsule | 2010-05-06 | 0000-00-00 | No | No | Current |