Minoxidil
- Product NDC
- 68016-382
- 11-digit product format
- 680160382
- Labeler code
- 68016
- Product ID
- 68016-382_a983c6de-98de-42ce-883e-7a1a78e86b09
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- ANDA075518
- Marketing category
- ANDA
- Marketing start
- 2003-09-11
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68016-382-00 | 68016038200 | 2 BOTTLE, DROPPER in 1 CARTON (68016-382-00) > 60 mL in 1 BOTTLE, DROPPER | 2003-09-11 | 0000-00-00 | No | No | Current |