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"57664-652-88" National Drug Code (NDC)
Labetalol 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-652-88)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-652-88
Package Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-652-88)
Product NDC
57664-652
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol
Non-Proprietary Name
Labetalol
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19990729
Marketing Category Name
ANDA
Application Number
ANDA075215
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
LABETALOL
Strength
300
Strength Unit
mg/1
Pharmacy Classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-652-88