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"58657-907-01" National Drug Code (NDC)
Labetalol Hydrochloride 100 BLISTER PACK in 1 CARTON (58657-907-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (58657-907-10)
(Method Pharmaceuticals, LLC)
NDC Code
58657-907-01
Package Description
100 BLISTER PACK in 1 CARTON (58657-907-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (58657-907-10)
Product NDC
58657-907
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
20250701
Marketing Category Name
ANDA
Application Number
ANDA075215
Manufacturer
Method Pharmaceuticals, LLC
Substance Name
LABETALOL
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/58657-907-01