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- Product NDC
- 11673-798
- 11-digit product format
- 116730798
- Labeler code
- 11673
- Product ID
- 11673-798_0603a8d1-b2e4-48e9-81e8-ad5563a3ef7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2021-06-03
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 3 g/60mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5965120SH1 | MINOXIDIL | 38304-91-5 | MINOXIDIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-798-30 | 11673079830 | 3 BOTTLE, DROPPER in 1 CARTON (11673-798-30) > 60 mL in 1 BOTTLE, DROPPER | 2021-06-03 | 0000-00-00 | No | No | Current |