Phentermine Hydrochloride
- Product NDC
- 72162-1628
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040526
- Marketing category
- ANDA
- Substance
- PHENTERMINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-1628-0 | 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1628-0) | 2023-09-27 | | No | Historical |
| 72162-1628-1 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1628-1) | 2023-09-27 | | No | Historical |
| 72162-1628-3 | 30 TABLET in 1 BOTTLE, PLASTIC (72162-1628-3) | 2023-09-27 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phentermine Hydrochloride | Bryant Ranch Prepack | 2023-09-27 | HUMAN PRESCRIPTION DRUG LABEL | 103 |