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"68001-561-17" National Drug Code (NDC)

Guaifenesin 8 BLISTER PACK in 1 CARTON (68001-561-17) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68001-561-16)
(BluePoint Laboratories)

NDC Code68001-561-17
Package Description8 BLISTER PACK in 1 CARTON (68001-561-17) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68001-561-16)
Product NDC68001-561
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230315
Marketing Category NameANDA
Application NumberANDA210453
ManufacturerBluePoint Laboratories
Substance NameGUAIFENESIN
Strength600
Strength Unitmg/1
Pharmacy ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-561-17





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