Minoxidil
- Product NDC
- 37808-202
- 11-digit product format
- 378080202
- Labeler code
- 37808
- Product ID
- 37808-202_d2915eda-7964-475a-9a86-088b194eadb8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- H E B
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2011-04-04
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-202-16 | 37808020216 | 1 BOTTLE in 1 CARTON (37808-202-16) > 60 mL in 1 BOTTLE | 1 bottle | 2011-04-28 | 0000-00-00 | No | No | Current |
| 37808-202-30 | 37808020230 | 3 BOTTLE in 1 CARTON (37808-202-30) > 60 mL in 1 BOTTLE | 3 bottle | 2011-04-04 | 0000-00-00 | No | No | Current |