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"51660-333-01" National Drug Code (NDC)

Arthritis Pain Reliever 1 BOTTLE in 1 CARTON (51660-333-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(Ohm Laboratories Inc.)

NDC Code51660-333-01
Package Description1 BOTTLE in 1 CARTON (51660-333-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC51660-333
Product Type NameHUMAN OTC DRUG
Proprietary NameArthritis Pain Reliever
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20020430
Marketing Category NameANDA
Application NumberANDA076200
ManufacturerOhm Laboratories Inc.
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-333-01





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