BOOST REGROWTH FOR WOMEN

Product NDC
10816-102
11-digit product format
108160102
Labeler code
10816
Product ID
10816-102_104718d1-9ec4-45a7-b8cb-f85cc555d942
Type
HUMAN OTC DRUG
Nonproprietary name
MINOXIDIL
Dosage form
LIQUID
Route
TOPICAL
Labeler
SHELBY PROFESSIONAL, INC.
Application
ANDA203932
Marketing category
ANDA
Marketing start
2012-03-01
Marketing end
0000-00-00
Substance
MINOXIDIL
Active strength
2 g/100mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10816-102-122019-11-13C16284748780-197449f38-d097-f6ea-e053-dbdaa90aa703beebddd0-9d67-455d-9c23-bcab964a5f35