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"49348-442-59" National Drug Code (NDC)

Sunmark Acid Reducer 4 BLISTER PACK in 1 CARTON (49348-442-59) > 10 TABLET, COATED in 1 BLISTER PACK
(McKesson)

NDC Code49348-442-59
Package Description4 BLISTER PACK in 1 CARTON (49348-442-59) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC49348-442
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Acid Reducer
Non-Proprietary NameFamotidine
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20030811
Marketing Category NameANDA
Application NumberANDA075312
ManufacturerMcKesson
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49348-442-59





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