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"29300-252-05" National Drug Code (NDC)
Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (29300-252-05)
(Unichem Pharmaceuticals (USA), Inc.)
NDC Code
29300-252-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (29300-252-05)
Product NDC
29300-252
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hydrochloride
Non-Proprietary Name
Labetalol Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20221001
Marketing Category Name
ANDA
Application Number
ANDA212719
Manufacturer
Unichem Pharmaceuticals (USA), Inc.
Substance Name
LABETALOL HYDROCHLORIDE
Strength
100
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/29300-252-05