Minoxidil
- Product NDC
- 63629-2230
- 11-digit product format
- 636292230
- Labeler code
- 63629
- Product ID
- 63629-2230_b1a22c7f-8c77-4635-9b8b-da9d9b8ca168
- 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 |
|---|
| 63629-2230-1 | 63629223001 | 100 TABLET in 1 BOTTLE (63629-2230-1) | 100 tablet | 2021-03-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Minoxidil | Bryant Ranch Prepack | 2024-08-19 | HUMAN PRESCRIPTION DRUG LABEL | 103 |