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"70710-1007-8" National Drug Code (NDC)

Misoprostol 120 TABLET in 1 BOTTLE (70710-1007-8)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code70710-1007-8
Package Description120 TABLET in 1 BOTTLE (70710-1007-8)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-1007-8





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