Phentermine Hydrochloride
- Product NDC
- 63629-1043
- 11-digit product format
- 636291043
- Labeler code
- 63629
- Product ID
- 63629-1043_8dc12309-8c44-4655-be73-b30313738357
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202248
- Marketing category
- ANDA
- Marketing start
- 2012-02-17
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 63629-1043-1 | 63629104301 | 1000 CAPSULE in 1 BOTTLE (63629-1043-1) | 1000 capsule | 2019-07-01 | 0000-00-00 | No | No | Current |