Sprintec
Sprintec (norgestimate and ethinylestradiol tablets)Rx only
Approved
Approval ID
e2f5ed4f-dd97-4dda-83d1-f8edd8786c0e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 17, 2011
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Norgestimate and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-769
Application NumberANDA075804
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norgestimate and Ethinyl Estradiol
Product Specifications
Effective DateOctober 27, 2009
FDA Product Classification