Phentermine Hydrochloride
- Product NDC
- 70934-474
- 11-digit product format
- 709340474
- Labeler code
- 70934
- Product ID
- 70934-474_b789bb6c-31e7-1908-e053-2a95a90aa7dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA040526
- Marketing category
- ANDA
- Marketing start
- 2019-12-18
- 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
- 2022-12-31
- 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 |
|---|
| 70934-474-30 | 70934047430 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-474-30) | 30 tablet | 2019-12-18 | 0000-00-00 | No | No | Current |
| 70934-474-90 | 70934047490 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-474-90) | 90 tablet | 2020-12-15 | 0000-00-00 | No | No | Current |