Minoxidil
- Product NDC
- 71335-3120
- 11-digit product format
- 713353120
- Labeler code
- 71335
- Product ID
- 71335-3120_84430a53-9161-415a-bc10-94e2b6df1d62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071345
- Marketing category
- ANDA
- Marketing start
- 2009-10-26
- Substance
- MINOXIDIL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Minoxidil
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 197986 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-3120-1 | Minoxidil | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 71335-3120-2 | 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 |
|---|
| 71335-3120-1 | 71335312001 | 100 TABLET in 1 BOTTLE (71335-3120-1) | 100 tablet | 2026-04-13 | No | No | Historical |
| 71335-3120-2 | 71335312002 | 30 TABLET in 1 BOTTLE (71335-3120-2) | 30 tablet | 2026-04-13 | No | No | Historical |