Levora
LEVORA 0.15/30-28 (levonorgestrel 0.15 mg and ethinyl estradiol 0.03 mg tablets)
Approved
Approval ID
0f2abab7-6dbe-4b18-b001-002b668eb370
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 7, 2023
Manufacturers
FDA
RPK Pharmaceuticals, Inc.
DUNS: 147096275
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
levonorgestrel and ethinyl estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code53002-1565
Application NumberANDA073594
Product Classification
M
Marketing Category
C73584
G
Generic Name
levonorgestrel and ethinyl estradiol
Product Specifications
Effective DateMarch 3, 2022
FDA Product Classification