Application 075844

Type
ANDA
Sponsor
SUN PHARM INDS INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001OXAPROZINOXAPROZINTABLET;ORAL600MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
57664-391OxaprozinOxaprozinCaraco Pharmaceutical Laboratories, Ltd.ANDACurrent
61919-178OXAPROZINOXAPROZINDIRECT RXANDACurrent
61919-178OXAPROZINOXAPROZINDIRECT RXANDACurrent