Home NDC 10816-102 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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 10816-102-12 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 10816-102-12 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 10816-102-12 110d247fa046…a55b01930146…
Source provenance: Browse the complete Orange Book source catalog .
FDA-Initiated Inactive NDC Indexing#