"43598-009-25" National Drug Code (NDC)

Guaifenesin 1200 Mg 2 BLISTER PACK in 1 CARTON (43598-009-25) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-009-74)
(Dr. Reddy's Laboratories Inc.)

NDC Code43598-009-25
Package Description2 BLISTER PACK in 1 CARTON (43598-009-25) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-009-74)
Product NDC43598-009
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin 1200 Mg
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220315
Marketing Category NameANDA
Application NumberANDA215932
ManufacturerDr. Reddy's Laboratories Inc.
Substance NameGUAIFENESIN
Strength1200
Strength Unitmg/1
Pharmacy ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]

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