Phentermine hydrochloride
- Product NDC
- 71335-2296
- 11-digit product format
- 713352296
- Labeler code
- 71335
- Product ID
- 71335-2296_e3949592-b026-44fe-83c9-0371a6db5adc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phentermine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205017
- Marketing category
- ANDA
- Marketing start
- 2017-01-24
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 37.5 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phentermine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENTERMINE HYDROCHLORIDE | 37.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0K2I505OTV |
| Rxcui | 803348 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2296-1 | Phentermine hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2296 | PHENTERMINE HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20250228_70f68311-8d1f-4b8e-b8a7-13bc4c17727e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2296-1 | 71335229601 | 100 CAPSULE in 1 BOTTLE (71335-2296-1) | 100 capsule | 2025-01-31 | No | No | Historical |