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"52125-756-02" National Drug Code (NDC)
Labetalol Hcl 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-756-02)
(REMEDYREPACK INC.)
NDC Code
52125-756-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (52125-756-02)
Product NDC
52125-756
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hcl
Non-Proprietary Name
Labetalol Hcl
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20131029
Marketing Category Name
ANDA
Application Number
ANDA075113
Manufacturer
REMEDYREPACK INC.
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/52125-756-02