PIRMELLA 7/7/7
Pirmella™ 7/7/7 and Pirmella™ 1/35 Tablets
Approved
Approval ID
1d34bba2-6223-46cb-a83f-ebb9145626be
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 20, 2022
Manufacturers
FDA
Lupin Pharmaceuticals, Inc.
DUNS: 089153071
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
NORETHINDRONE AND ETHINYL ESTRADIOL
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68180-892
Application NumberANDA201510
Product Classification
M
Marketing Category
C73584
G
Generic Name
NORETHINDRONE AND ETHINYL ESTRADIOL
Product Specifications
Effective DateDecember 20, 2022
FDA Product Classification
NORETHINDRONE AND ETHINYL ESTRADIOL
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68180-893
Application NumberANDA201512
Product Classification
M
Marketing Category
C73584
G
Generic Name
NORETHINDRONE AND ETHINYL ESTRADIOL
Product Specifications
Effective DateDecember 20, 2022
FDA Product Classification