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"31722-805-01" National Drug Code (NDC)

Tolterodine Tartrate 10 BLISTER PACK in 1 CARTON (31722-805-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-31)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-805-01
Package Description10 BLISTER PACK in 1 CARTON (31722-805-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-31)
Product NDC31722-805
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTolterodine Tartrate
Non-Proprietary NameTolterodine Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210802
Marketing Category NameANDA
Application NumberANDA204397
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameTOLTERODINE TARTRATE
Strength1
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/31722-805-01





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