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NDC 79903-072, Minoxidil, solution, from WALMART INC..
- Product NDC
- 79903-072
- Status
- Listed
- Labeler
- WALMART INC.
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA075357
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/79903-072 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOXIDIL2 g/100mL
Pharmacologic classes
Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 79903-072-30 | 79903007230 | 3 BOTTLE, WITH APPLICATOR in 1 CARTON (79903-072-30) / 60 mL in 1 BOTTLE, WITH APPLICATOR |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 79903-072 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/79903-072 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 79903-072. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.