minoxidil
- Product NDC
- 37808-798
- 11-digit product format
- 378080798
- Labeler code
- 37808
- Product ID
- 37808-798_838e8952-5079-4b72-9f33-d5b9a457c6a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- H E B
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2010-02-16
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 3 g/60mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-798 | MINOXIDIL FOR MEN (MINOXIDIL) SOLUTION [H E B] | 5 | Legacy NDC | 20210805_81489e33-92be-45a5-9fa1-b352b640340b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-798-16 | 37808079816 | 1 BOTTLE, DROPPER in 1 CARTON (37808-798-16) > 60 mL in 1 BOTTLE, DROPPER | 2010-06-16 | 0000-00-00 | No | No | Current |
| 37808-798-30 | 37808079830 | 3 BOTTLE, DROPPER in 1 CARTON (37808-798-30) > 60 mL in 1 BOTTLE, DROPPER | 2010-02-16 | 0000-00-00 | No | No | Current |