Up and Up minoxidil
- Product NDC
- 11673-856
- 11-digit product format
- 116730856
- Labeler code
- 11673
- Product ID
- 11673-856_6ade6331-f2df-4edc-9e56-f756998cbe9d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2009-05-27
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 11673-856-30 | ML - Milliliter | 11673-856 | 203f668a-2829-46a2-9f45-a6cbeb2e15b7 | 1 | 2015-07-20 |