Minoxidil Topical Solution USP, 2%
- Product NDC
- 87532-001
- 11-digit product format
- 875320001
- Labeler code
- 87532
- Product ID
- 87532-001_4d65a174-ad6f-3f0a-e063-6294a90a132a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil 2%
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Carol's Daughter, LLC
- Application
- ANDA078176
- Marketing category
- ANDA
- Marketing start
- 2026-04-03
- Substance
- MINOXIDIL
- Active strength
- .02 g/mL
- 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 Topical Solution USP, 2%
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | .02 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 311723 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87532-001-01 | Minoxidil Topical Solution USP, 2% | 60 mL in 1 BOTTLE | SOLUTION | 60 | | 1 |
| 87532-001-01 | Minoxidil Topical Solution USP, 2% | 1 in 1 BOX | SOLUTION | 1 | | 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 |
|---|
| 87532-001-01 | 87532000101 | 1 BOTTLE in 1 BOX (87532-001-01) / 60 mL in 1 BOTTLE | 1 bottle | 2026-04-03 | No | No | Current |