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"51672-2151-9" National Drug Code (NDC)
Minoxidil Topical Solution, 5% 3 BOTTLE in 1 CARTON (51672-2151-9) / 60 mL in 1 BOTTLE
(Sun Pharmaceutical Industries, Inc.)
NDC Code
51672-2151-9
Package Description
3 BOTTLE in 1 CARTON (51672-2151-9) / 60 mL in 1 BOTTLE
Product NDC
51672-2151
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Minoxidil Topical Solution, 5%
Non-Proprietary Name
Minoxidil Solution
Dosage Form
SOLUTION
Usage
TOPICAL
Start Marketing Date
20250801
Marketing Category Name
ANDA
Application Number
ANDA217998
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
MINOXIDIL
Strength
50
Strength Unit
mg/mL
Pharmacy Classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-2151-9