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"51645-705-10" National Drug Code (NDC)

Pluspharma Extra Strength 1000 TABLET in 1 BOTTLE, PLASTIC (51645-705-10)
(Gemini Pharmaceuticals, Inc. dba Plus Pharma)

NDC Code51645-705-10
Package Description1000 TABLET in 1 BOTTLE, PLASTIC (51645-705-10)
Product NDC51645-705
Product Type NameHUMAN OTC DRUG
Proprietary NamePluspharma Extra Strength
Proprietary Name SuffixPain Reliever,fever Reducer 500 Mg
Non-Proprietary NameAcetaminophen
Dosage FormTABLET
UsageORAL
Start Marketing Date20060327
End Marketing Date20230531
Marketing Category NameOTC MONOGRAPH NOT FINAL
Application Numberpart343
ManufacturerGemini Pharmaceuticals, Inc. dba Plus Pharma
Substance NameACETAMINOPHEN
Strength500
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51645-705-10





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