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"51660-057-12" National Drug Code (NDC)

Guaifenesin And Pseudoephedrine Hcl 1 BLISTER PACK in 1 CARTON (51660-057-12) > 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Ohm Laboratories, Inc.)

NDC Code51660-057-12
Package Description1 BLISTER PACK in 1 CARTON (51660-057-12) > 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC51660-057
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin And Pseudoephedrine Hcl
Non-Proprietary NameGuaifenesin And Pseudoephedrine Hcl
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210401
Marketing Category NameANDA
Application NumberANDA212542
ManufacturerOhm Laboratories, Inc.
Substance NameGUAIFENESIN; PSEUDOEPHEDRINE
Strength1200; 120
Strength Unitmg/1; mg/1
Pharmacy ClassesAdrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]

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