keeps minoxidil topical
- Product NDC
- 71713-093
- 11-digit product format
- 717130093
- Labeler code
- 71713
- Product ID
- 71713-093_4e687416-751c-4369-8d89-a4a434ad040c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- THIRTY MADISON INC
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2019-05-31
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 3 g/60mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71713-093-30 | 71713009330 | 3 BOTTLE in 1 CARTON (71713-093-30) > 60 mL in 1 BOTTLE | 3 bottle | 2019-05-31 | 0000-00-00 | No | No | Current |