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"57664-141-34" National Drug Code (NDC)

Ranitidine 473 mL in 1 BOTTLE (57664-141-34)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-141-34
Package Description473 mL in 1 BOTTLE (57664-141-34)
Product NDC57664-141
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormSYRUP
UsageORAL
Start Marketing Date20111003
Marketing Category NameANDA
Application NumberANDA091091
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameRANITIDINE HYDROCHLORIDE
Strength15
Strength Unitmg/mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-141-34





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