"70748-332-02" National Drug Code (NDC)

Prednisolone Acetate 1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLE
(Lupin Pharmaceuticals, Inc.)

NDC Code70748-332-02
Package Description1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLE
Product NDC70748-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisolone Acetate
Non-Proprietary NamePrednisolone Acetate
Dosage FormSUSPENSION/ DROPS
UsageOPHTHALMIC
Start Marketing Date20241011
Marketing Category NameANDA
Application NumberANDA216935
ManufacturerLupin Pharmaceuticals, Inc.
Substance NamePREDNISOLONE ACETATE
Strength10
Strength Unitmg/mL
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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