minoxidil
- Product NDC
- 11822-0798
- 11-digit product format
- 118220798
- Labeler code
- 11822
- Product ID
- 11822-0798_7d7018c2-f65c-4284-98a5-a90e2f3bd479
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2016-08-18
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 3 g/60mL
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0798 | MINOXIDIL SOLUTION [RITE AID CORPORATION] | 5 | Legacy NDC | 20220309_adfff764-e29f-4aa5-b8f2-185e88ec8ac5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0798-1 | 11822079801 | 3 BOTTLE in 1 CARTON (11822-0798-1) > 60 mL in 1 BOTTLE | 3 bottle | 2016-08-18 | 0000-00-00 | No | No | Current |
| 11822-0798-2 | 11822079802 | 1 BLISTER PACK in 1 CARTON (11822-0798-2) > 60 mL in 1 BLISTER PACK | 1 blister pack | 2020-09-18 | 0000-00-00 | No | No | Current |