Shapiro MD 5% Minoxidil Hair Regrowth Treatment for Men

Product NDC
73277-001
11-digit product format
732770001
Labeler code
73277
Product ID
73277-001_f1e96883-af8e-3cb9-e053-2995a90abee2
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
SOLUTION
Route
TOPICAL
Labeler
CONVERSION LABS PR, LLC
Application
ANDA076239
Marketing category
ANDA
Marketing start
2019-07-28
Marketing end
0000-00-00
Substance
MINOXIDIL
Active strength
5 mg/100mL
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2024-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73277-001-012025-01-30C16284748780-12cef2736-a429-d83d-e063-dadaa90ab31fShapiro MD 5% Minoxidil Hair Regrowth Treatment for Men

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73277-001-01Shapiro MD 5% Minoxidil Hair Regrowth Treatment for Men60 mL in 1 BOTTLESOLUTION602
73277-001-01Shapiro MD 5% Minoxidil Hair Regrowth Treatment for Men1 in 1 BOXSOLUTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73277-001SHAPIRO MD 5% MINOXIDIL HAIR REGROWTH TREATMENT FOR MEN (MINOXIDIL) SOLUTION [CONVERSION LABS PR, LLC]2Legacy NDC, 2 package rows20230111_8ec09b28-7f2c-ee32-e053-2995a90a3331.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73277-001-01732770001011 BOTTLE in 1 BOX (73277-001-01) > 60 mL in 1 BOTTLE1 bottle2019-07-280000-00-00NoNoCurrent