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"68001-206-03" National Drug Code (NDC)
Labetalol Hcl 500 TABLET, FILM COATED in 1 BOTTLE (68001-206-03)
(BluePoint Laboratories)
NDC Code
68001-206-03
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (68001-206-03)
Product NDC
68001-206
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
20140226
End Marketing Date
20210430
Marketing Category Name
ANDA
Application Number
ANDA075113
Manufacturer
BluePoint Laboratories
Substance Name
LABETALOL HYDROCHLORIDE
Strength
300
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/68001-206-03