Phentermine Hydrochloride
- Product NDC
- 50436-9029
- 11-digit product format
- 504369029
- Labeler code
- 50436
- Product ID
- 50436-9029_24b06cb9-5212-4858-91a1-a867504eda97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040886
- Marketing category
- ANDA
- Marketing start
- 2012-08-07
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 15 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
- 2020-12-31
- 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 |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phentermine Hydrochloride | Unit Dose Services | 2023-08-28 | HUMAN PRESCRIPTION DRUG LABEL | 7 |