Phentermine Hydrochloride
- Product NDC
- 50436-3174
- 11-digit product format
- 504363174
- Labeler code
- 50436
- Product ID
- 50436-3174_c4ad2282-304c-4199-b27b-ce00fbd8c6ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040525
- Marketing category
- ANDA
- Marketing start
- 2003-10-23
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-3174-1 | Phentermine Hydrochloride | 21 in 1 BOTTLE | CAPSULE | 21 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3174 | PHENTERMINE HYDROCHLORIDE CAPSULE [UNIT DOSE SERVICES] | 6 | Legacy NDC, 1 package rows | 20171108_64f6640a-6811-439e-b9a1-ad04fe77e694.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3174-1 | 50436317401 | 21 in 1 BOTTLE | Historical |