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"71335-0949-6" National Drug Code (NDC)
Baclofen 30 TABLET in 1 BOTTLE (71335-0949-6)
(Bryant Ranch Prepack)
NDC Code
71335-0949-6
Package Description
30 TABLET in 1 BOTTLE (71335-0949-6)
Product NDC
71335-0949
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Baclofen
Non-Proprietary Name
Baclofen
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180401
Marketing Category Name
ANDA
Application Number
ANDA209102
Manufacturer
Bryant Ranch Prepack
Substance Name
BACLOFEN
Strength
20
Strength Unit
mg/1
Pharmacy Classes
GABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0949-6