Phentermine Hydrochloride
- Product NDC
- 72789-208
- 11-digit product format
- 727890208
- Labeler code
- 72789
- Product ID
- 72789-208_e66191a6-0c39-7319-e053-2a95a90aae84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA200272
- Marketing category
- ANDA
- Marketing start
- 2011-03-08
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 38 mg/1
- Pharmacologic classes
- Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0K2I505OTV | PHENTERMINE HYDROCHLORIDE | 1197-21-3 | PHENTERMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-208-01 | 72789020801 | 100 TABLET in 1 BOTTLE, PLASTIC (72789-208-01) | 100 tablet | 2021-11-03 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phentermine Hydrochloride | PD-Rx Pharmaceuticals, Inc. | 2024-01-18 | HUMAN PRESCRIPTION DRUG LABEL | 12 |