KERANIQUE For Women Hair Regrowth Treatment
- Product NDC
- 65121-562
- 11-digit product format
- 651210562
- Labeler code
- 65121
- Product ID
- 65121-562_48309692-0dbf-5e6b-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MINOXIDIL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pure Source, LLC
- Application
- ANDA078176
- Marketing category
- ANDA
- Marketing start
- 2014-02-06
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 65121-562-02 | 65121056202 | 1 BOTTLE, DROPPER in 1 CARTON (65121-562-02) > 60 mL in 1 BOTTLE, DROPPER | 2017-02-10 | 0000-00-00 | No | No | Current |