Phentermine Hydrochloride
- Product NDC
- 50090-1499
- 11-digit product format
- 500901499
- Labeler code
- 50090
- Product ID
- 50090-1499_4f696981-5925-4438-a5a9-00715fb27b01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040526
- Marketing category
- ANDA
- Marketing start
- 2013-08-12
- 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
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 |
|---|
| 50090-1499-2 | Phentermine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1499 | PHENTERMINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 1 package rows | 20210224_77c5941e-49ca-4b60-9743-14192bdc3e2f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1499-2 | 50090149902 | 100 TABLET in 1 BOTTLE (50090-1499-2) | 100 tablet | 2014-12-05 | 0000-00-00 | No | No | Current |