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"51660-072-86" National Drug Code (NDC)

Guaifenesin 2 BLISTER PACK in 1 CARTON (51660-072-86) > 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(OHM LABORATORIES INC)

NDC Code51660-072-86
Package Description2 BLISTER PACK in 1 CARTON (51660-072-86) > 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC51660-072
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Proprietary Name SuffixExtended Release
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20171210
Marketing Category NameNDA
Application NumberNDA021282
ManufacturerOHM LABORATORIES INC
Substance NameGUAIFENESIN
Strength1200
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-072-86





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