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"72603-903-02" National Drug Code (NDC)
Labetalol Hydrochloride 500 TABLET in 1 BOTTLE (72603-903-02)
(NorthStar Rx LLC)
NDC Code
72603-903-02
Package Description
500 TABLET in 1 BOTTLE (72603-903-02)
Product NDC
72603-903
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hydrochloride
Non-Proprietary Name
Labetalol Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20260319
Marketing Category Name
ANDA
Application Number
ANDA074787
Manufacturer
NorthStar Rx LLC
Substance Name
LABETALOL HYDROCHLORIDE
Strength
200
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/72603-903-02