"0121-0727-16" National Drug Code (NDC)

Ranitidine 473 mL in 1 BOTTLE (0121-0727-16)
(Pharmaceutical Associates, Inc.)

NDC Code0121-0727-16
Package Description473 mL in 1 BOTTLE (0121-0727-16)
Product NDC0121-0727
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormSYRUP
UsageORAL
Start Marketing Date20101101
Marketing Category NameANDA
Application NumberANDA077405
ManufacturerPharmaceutical Associates, Inc.
Substance NameRANITIDINE
Strength15
Strength Unitmg/mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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