Phentermine Hydrochloride
- Product NDC
- 50090-3535
- 11-digit product format
- 500903535
- Labeler code
- 50090
- Product ID
- 50090-3535_b0500b2a-e3bf-44ab-84fd-a1a062d3732a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA087022
- Marketing category
- ANDA
- Marketing start
- 2007-12-01
- 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 |
|---|
| 50090-3535-2 | Phentermine Hydrochloride | 90 in 1 BOTTLE | CAPSULE | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3535 | PHENTERMINE HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20210417_3e5b49f1-314d-4d3c-9278-1c6880789bf6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3535-2 | 50090353502 | 90 CAPSULE in 1 BOTTLE (50090-3535-2) | 90 capsule | 2018-08-13 | 0000-00-00 | No | No | Current |