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"51660-070-21" National Drug Code (NDC)

Guaifenesin 1 BLISTER PACK in 1 CARTON (51660-070-21) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(OHM LABORATORIES INC)

NDC Code51660-070-21
Package Description1 BLISTER PACK in 1 CARTON (51660-070-21) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC51660-070
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180108
Marketing Category NameNDA
Application NumberNDA021282
ManufacturerOHM LABORATORIES INC
Substance NameGUAIFENESIN
Strength600
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-070-21





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