minoxidil
- Product NDC
- 37808-833
- 11-digit product format
- 378080833
- Labeler code
- 37808
- Product ID
- 37808-833_4c5ad951-ff69-440e-98d0-feb87923cc33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- H E B
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2021-05-17
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 37808-833-16 | 37808083316 | 1 BOTTLE, DROPPER in 1 CARTON (37808-833-16) / 60 mL in 1 BOTTLE, DROPPER | 2021-05-17 | No | No | Historical |
| 37808-833-30 | 37808083330 | 3 BOTTLE, DROPPER in 1 CARTON (37808-833-30) / 60 mL in 1 BOTTLE, DROPPER | 2021-05-17 | No | No | Historical |