Phentermine Hydrochloride
- Product NDC
- 70518-3407
- 11-digit product format
- 705183407
- Labeler code
- 70518
- Product ID
- 70518-3407_dc26d935-195f-6ab8-e053-2995a90ac4f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040876
- Marketing category
- ANDA
- Marketing start
- 2022-04-08
- 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 |
|---|
| 70518-3407-0 | 70518340700 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-3407-0) | 30 tablet | 2022-04-08 | 0000-00-00 | No | No | Current |