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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Minoxidil
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 197987 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-240-30 | Minoxidil | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |