Minoxidil
- Product NDC
- 0363-9972
- 11-digit product format
- 003639972
- Labeler code
- 0363
- Product ID
- 0363-9972_15e75998-fefa-4bbe-8959-d6ff53b21b14
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Walgreens
- Application
- ANDA074588
- Marketing category
- ANDA
- Marketing start
- 2022-10-14
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-9972-06 | 00363997206 | 3 BOTTLE, DROPPER in 1 CARTON (0363-9972-06) > 60 mL in 1 BOTTLE, DROPPER | 2022-10-14 | 0000-00-00 | No | No | Current |