SHAROBEL
SHAROBEL™(Norethindrone Tablets, USP)
Approved
Approval ID
a96f5194-ad2a-4783-a9a9-22a288caff25
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 30, 2023
Manufacturers
FDA
Northstar Rx LLC
DUNS: 830546433
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Norethindrone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16714-441
Application NumberANDA200961
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norethindrone
Product Specifications
Effective DateMay 23, 2016
FDA Product Classification