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"61786-393-02" National Drug Code (NDC)
Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-393-02)
(REMEDYREPACK INC.)
NDC Code
61786-393-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (61786-393-02)
Product NDC
61786-393
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
20150812
Marketing Category Name
ANDA
Application Number
ANDA075133
Manufacturer
REMEDYREPACK 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/61786-393-02