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"60687-450-01" National Drug Code (NDC)
Labetalol Hydrochloride 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-450-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-450-11)
(American Health Packaging)
NDC Code
60687-450-01
Package Description
100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-450-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-450-11)
Product NDC
60687-450
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
20190716
Marketing Category Name
ANDA
Application Number
ANDA207743
Manufacturer
American Health Packaging
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/60687-450-01