Minoxidil For Men
- Product NDC
- 70550-503
- 11-digit product format
- 705500503
- Labeler code
- 70550
- Product ID
- 70550-503_730d6693-0bf5-43ec-8ea3-44af586ee282
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Atlantic Coast Media Group, LLC
- Application
- ANDA075518
- Marketing category
- ANDA
- Marketing start
- 2020-04-04
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70550-503-01 | 70550050301 | 1 BOTTLE in 1 CARTON (70550-503-01) > 60 mL in 1 BOTTLE | 1 bottle | 2020-04-04 | 0000-00-00 | No | No | Current |