minoxidil - 37808-798-16 - (Minoxidil)

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Drug Information of minoxidil

Product NDC: 37808-798
Proprietary Name: minoxidil
Non Proprietary Name: Minoxidil
Active Ingredient(s): 3    g/60mL & nbsp;   Minoxidil
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of minoxidil

Product NDC: 37808-798
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075598
Marketing Category: ANDA
Start Marketing Date: 20100216

Package Information of minoxidil

Package NDC: 37808-798-16
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (37808-798-16) > 60 mL in 1 BOTTLE, DROPPER

NDC Information of minoxidil

NDC Code 37808-798-16
Proprietary Name minoxidil
Package Description 1 BOTTLE, DROPPER in 1 CARTON (37808-798-16) > 60 mL in 1 BOTTLE, DROPPER
Product NDC 37808-798
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Minoxidil
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20100216
Marketing Category Name ANDA
Labeler Name H E B
Substance Name MINOXIDIL
Strength Number 3
Strength Unit g/60mL
Pharmaceutical Classes

Complete Information of minoxidil


General Information