Minoxidil
- Product NDC
- 72162-1490
- 11-digit product format
- 721621490
- Labeler code
- 72162
- Product ID
- 72162-1490_04276eed-6d51-6906-e063-6294a90a5a06
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 72162-1490-5 | 72162149005 | 500 TABLET in 1 BOTTLE (72162-1490-5) | 500 tablet | 2023-04-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Minoxidil | Bryant Ranch Prepack | 2023-08-30 | HUMAN PRESCRIPTION DRUG LABEL | 101 |