Phentermine Hydrochloride
- Product NDC
- 68071-3816
- 11-digit product format
- 680713816
- Labeler code
- 68071
- Product ID
- 68071-3816_312da1f3-1909-cc1d-e063-6394a90adc5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040526
- Marketing category
- ANDA
- Marketing start
- 2013-08-12
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 30 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 68071-3816-1 | 68071381601 | 1000 TABLET in 1 BOTTLE, PLASTIC (68071-3816-1) | 1000 tablet | 2025-03-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phentermine Hydrochloride | NuCare Pharmaceuticals,Inc. | 2025-03-25 | HUMAN PRESCRIPTION DRUG LABEL | 1 |