ELEVATE 5% MINOXIDIL FOAM
- Product NDC
- 78098-301
- 11-digit product format
- 780980301
- Labeler code
- 78098
- Product ID
- 78098-301_dab41d8a-196e-9d81-e053-2995a90a49e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ELEVATE 5% MINOXIDIL FOAM
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- GUANGZHOU NODA PHARMACEUTICAL TECHNOLOGY INCORPORATED CO., LTD
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2022-04-01
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 5 g/100g
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 78098-301-01 | 78098030101 | 60 g in 1 BOTTLE, PUMP (78098-301-01) | 60 g | 2022-04-01 | 0000-00-00 | No | No | Current |