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"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 Code
70748-332-02
Package Description
1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLE
Product NDC
70748-332
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisolone Acetate
Non-Proprietary Name
Prednisolone Acetate
Dosage Form
SUSPENSION/ DROPS
Usage
OPHTHALMIC
Start Marketing Date
20241011
Marketing Category Name
ANDA
Application Number
ANDA216935
Manufacturer
Lupin Pharmaceuticals, Inc.
Substance Name
PREDNISOLONE ACETATE
Strength
10
Strength Unit
mg/mL
Pharmacy Classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70748-332-02