Michiru hair regrowth treatment for women
- Product NDC
- 64942-2110
- 11-digit product format
- 649422110
- Labeler code
- 64942
- Product ID
- 64942-2110_2044253c-bd77-452d-a57c-51152dc8040e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Conopco Inc. d/b/a Unilever
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2022-12-14
- 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
- 2024-12-31
- 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 |
|---|
| 64942-2110 | MICHIRU HAIR REGROWTH TREATMENT FOR WOMEN (MINOXIDIL) SOLUTION [CONOPCO INC. D/B/A UNILEVER] | 1 | Legacy NDC | 20230110_2044253c-bd77-452d-a57c-51152dc8040e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64942-2110-1 | 64942211001 | 1 BOTTLE, DROPPER in 1 CARTON (64942-2110-1) > 60 mL in 1 BOTTLE, DROPPER | 2022-12-14 | 0000-00-00 | No | No | Current |