minoxidil
- Product NDC
- 37808-404
- 11-digit product format
- 378080404
- Labeler code
- 37808
- Product ID
- 37808-404_9f0496c3-31df-420f-830f-76165089d681
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- H E B
- Application
- ANDA091344
- Marketing category
- ANDA
- Marketing start
- 2012-03-01
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 37808-404-01 | 37808040401 | 1 CAN in 1 CARTON (37808-404-01) > 60 g in 1 CAN | 1 can | 2012-03-01 | 0000-00-00 | No | No | Current |
| 37808-404-03 | 37808040403 | 3 CAN in 1 CARTON (37808-404-03) > 60 g in 1 CAN | 3 can | 2012-03-01 | 0000-00-00 | No | No | Current |