hair regrowth treatment
- Product NDC
- 21130-611
- 11-digit product format
- 211300611
- Labeler code
- 21130
- Product ID
- 21130-611_4eaefc19-eda6-46e4-a56e-93a1787e4bd2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Safeway
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2024-08-13
- Substance
- MINOXIDIL
- Active strength
- 5 g/100mL
- 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 |
|---|
| 21130-611-16 | 21130061116 | 1 BOTTLE in 1 CARTON (21130-611-16) / 60 mL in 1 BOTTLE | 1 bottle | 2024-08-13 | No | No | Historical |
| 21130-611-30 | 21130061130 | 3 BOTTLE in 1 CARTON (21130-611-30) / 60 mL in 1 BOTTLE | 3 bottle | 2024-08-20 | No | No | Historical |