Capillus Hair Regrowth Treatment
- Product NDC
- 71176-781
- 11-digit product format
- 711760781
- Labeler code
- 71176
- Product ID
- 71176-781_4779865e-8ccc-2d96-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MINOXIDIL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Capillus, Llc
- Application
- ANDA076239
- Marketing category
- ANDA
- Marketing start
- 2017-01-24
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71176-781-02 | 71176078102 | 1 BOTTLE in 1 BOX (71176-781-02) > 60 mL in 1 BOTTLE | 1 bottle | 2017-01-24 | 0000-00-00 | No | No | Current |