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"31722-588-32" National Drug Code (NDC)
Nebivolol 10 BLISTER PACK in 1 CARTON (31722-588-32) / 10 TABLET in 1 BLISTER PACK (31722-588-31)
(Camber Pharmaceuticals, Inc.)
NDC Code
31722-588-32
Package Description
10 BLISTER PACK in 1 CARTON (31722-588-32) / 10 TABLET in 1 BLISTER PACK (31722-588-31)
Product NDC
31722-588
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nebivolol
Non-Proprietary Name
Nebivolol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20210917
Marketing Category Name
ANDA
Application Number
ANDA203825
Manufacturer
Camber Pharmaceuticals, Inc.
Substance Name
NEBIVOLOL HYDROCHLORIDE
Strength
20
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/31722-588-32