Minoxidil
- Product NDC
- 82804-240
- 11-digit product format
- 828040240
- Labeler code
- 82804
- Product ID
- 82804-240_a0066eac-cb58-49ef-a480-105cb1043c2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA071826
- Marketing category
- ANDA
- Marketing start
- 1988-11-14
- Substance
- MINOXIDIL
- Active strength
- 2.5 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 |
|---|
| 82804-240-30 | 82804024030 | 30 TABLET in 1 BOTTLE (82804-240-30) | 30 tablet | 2025-09-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Minoxidil Tablets, USP | Proficient Rx LP | 2025-09-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |