Minoxidil
- Product NDC
- 50090-7760
- 11-digit product format
- 500907760
- Labeler code
- 50090
- Product ID
- 50090-7760_9912a946-471e-4e0c-addf-373f401da0c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071839
- Marketing category
- ANDA
- Marketing start
- 1988-11-14
- Substance
- MINOXIDIL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5965120SH1 | MINOXIDIL | 38304-91-5 | MINOXIDIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7760-2 | 50090776002 | 90 TABLET in 1 BOTTLE (50090-7760-2) | 90 tablet | 2025-11-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Minoxidil Tablets, USP | A-S Medication Solutions | 2025-11-10 | HUMAN PRESCRIPTION DRUG LABEL | 2 |