Phentermine hydrochloride
- Product NDC
- 53002-7931
- 11-digit product format
- 530027931
- Labeler code
- 53002
- Product ID
- 53002-7931_acf1ff22-a4bd-4a06-af3b-a27835acd07d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phentermine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA205008
- Marketing category
- ANDA
- Marketing start
- 2017-01-24
- 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
- 2021-12-31
- 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 |
|---|
| 53002-7931-3 | 53002793103 | 30 TABLET in 1 BOTTLE (53002-7931-3) | 30 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |