"70710-1007-4" National Drug Code (NDC)

Misoprostol 10 BLISTER PACK in 1 CARTON (70710-1007-4) > 10 TABLET in 1 BLISTER PACK (70710-1007-2)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code70710-1007-4
Package Description10 BLISTER PACK in 1 CARTON (70710-1007-4) > 10 TABLET in 1 BLISTER PACK (70710-1007-2)
Product NDC70710-1007
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMisoprostol
Non-Proprietary NameMisoprostol
Dosage FormTABLET
UsageORAL
Start Marketing Date20200114
Marketing Category NameANDA
Application NumberANDA210201
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameMISOPROSTOL
Strength200
Strength Unitug/1
Pharmacy ClassesProstaglandin E1 Analog [EPC], Prostaglandins E, Synthetic [CS]

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