Phentermine Hydrochloride
- Product NDC
- 72162-2313
- 11-digit product format
- 721622313
- Labeler code
- 72162
- Product ID
- 72162-2313_5aa20f35-cd97-4e8e-9d9a-2b3905de0617
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202248
- Marketing category
- ANDA
- Marketing start
- 2024-02-15
- Marketing end
- 2028-04-30
- 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
- Current FDA listing
- Yes
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 |
|---|
| 72162-2313-0 | 72162231300 | 1000 CAPSULE in 1 BOTTLE (72162-2313-0) | 1000 capsule | 2024-05-13 | 2028-04-30 | No | No | Historical |
| 72162-2313-1 | 72162231301 | 100 CAPSULE in 1 BOTTLE (72162-2313-1) | 100 capsule | 2024-05-13 | 2028-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phentermine Hydrochloride | Bryant Ranch Prepack | 2025-12-29 | HUMAN PRESCRIPTION DRUG LABEL | 102 |