Minoxidil
- Product NDC
- 71205-757
- 11-digit product format
- 712050757
- Labeler code
- 71205
- Product ID
- 71205-757_637718aa-a453-4acd-a992-590d637b63a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA071344
- Marketing category
- ANDA
- Marketing start
- 2009-10-26
- 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
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 |
|---|
| 71205-757-30 | 71205075730 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-757-30) | 30 tablet | 2023-02-07 | No | No | Historical |
| 71205-757-60 | 71205075760 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-757-60) | 60 tablet | 2023-02-07 | No | No | Historical |
| 71205-757-90 | 71205075790 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-757-90) | 90 tablet | 2023-02-07 | No | No | Historical |