Phendimetrazine Tartrate
- Product NDC
- 68071-3839
- 11-digit product format
- 680713839
- Labeler code
- 68071
- Product ID
- 68071-3839_342bbef4-9066-b7df-e063-6294a90a8067
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phendimetrazine Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA091042
- Marketing category
- ANDA
- Marketing start
- 2010-09-15
- Substance
- PHENDIMETRAZINE TARTRATE
- Active strength
- 35 mg/1
- Pharmacologic classes
- Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6985IP0T80 | PHENDIMETRAZINE TARTRATE | 50-58-8 | PHENDIMETRAZINE TARTRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3839-9 | 68071383909 | 90 TABLET in 1 BOTTLE (68071-3839-9) | 90 tablet | 2025-05-02 | No | No | Historical |