Minoxidil
- Product NDC
- 59450-211
- 11-digit product format
- 594500211
- Labeler code
- 59450
- Product ID
- 59450-211_41419988-5dbf-4f47-92d0-0f6f6b6513e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Kroger Company
- Application
- ANDA209074
- Marketing category
- ANDA
- Marketing start
- 2022-10-18
- Substance
- MINOXIDIL
- Active strength
- 50 mg/g
- 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 |
|---|
| 59450-211-02 | 59450021102 | 2 CAN in 1 CARTON (59450-211-02) / 60 g in 1 CAN (59450-211-01) | 2 can | 2022-10-18 | No | No | Historical |