"51991-201-10" National Drug Code (NDC)

Folic Acid 1000 TABLET in 1 BOTTLE (51991-201-10)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-201-10
Package Description1000 TABLET in 1 BOTTLE (51991-201-10)
Product NDC51991-201
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFolic Acid
Non-Proprietary NameFolic Acid
Dosage FormTABLET
UsageORAL
Start Marketing Date20100420
End Marketing Date20140430
Marketing Category NameANDA
Application NumberANDA040796
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameFOLIC ACID
Strength1
Strength Unitmg/1

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