Phentermine Hydrochloride
- Product NDC
- 68071-3819
- 11-digit product format
- 680713819
- Labeler code
- 68071
- Product ID
- 68071-3819_315baaa6-5129-f27b-e063-6294a90a2c91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040876
- Marketing category
- ANDA
- Marketing start
- 2012-08-15
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 37.5 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 |
|---|
| 68071-3819-1 | 68071381901 | 1000 TABLET in 1 BOTTLE (68071-3819-1) | 1000 tablet | 2025-03-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phentermine Hydrochloride | NuCare Pharmaceuticals,Inc. | 2025-03-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |