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"58605-422-02" National Drug Code (NDC)

Maxiphen 20 TABLET in 1 BLISTER PACK (58605-422-02)
(MCR American Pharmaceuticals, Inc.)

NDC Code58605-422-02
Package Description20 TABLET in 1 BLISTER PACK (58605-422-02)
Product NDC58605-422
Product Type NameHUMAN OTC DRUG
Proprietary NameMaxiphen
Non-Proprietary NameGuaifenesin And Phenylephrine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20080331
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart341
ManufacturerMCR American Pharmaceuticals, Inc.
Substance NameGUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength400; 10
Strength Unitmg/1; mg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58605-422-02





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