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"70069-712-01" National Drug Code (NDC)

Bepotastine Besilate 1 BOTTLE in 1 CARTON (70069-712-01) / 10 mL in 1 BOTTLE
(Somerset Therapeutics, LLC)

NDC Code70069-712-01
Package Description1 BOTTLE in 1 CARTON (70069-712-01) / 10 mL in 1 BOTTLE
Product NDC70069-712
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBepotastine Besilate
Non-Proprietary NameBepotastine Besilate
Dosage FormSOLUTION
UsageOPHTHALMIC
Start Marketing Date20241010
Marketing Category NameANDA
Application NumberANDA217770
ManufacturerSomerset Therapeutics, LLC
Substance NameBEPOTASTINE BESILATE
Strength15
Strength Unitmg/mL
Pharmacy ClassesHistamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70069-712-01





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