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"70710-1021-8" National Drug Code (NDC)
Albendazole 1 BLISTER PACK in 1 BOTTLE (70710-1021-8) > 2 TABLET, FILM COATED in 1 BLISTER PACK
(Zydus Pharmaceuticals USA Inc.)
NDC Code
70710-1021-8
Package Description
1 BLISTER PACK in 1 BOTTLE (70710-1021-8) > 2 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
70710-1021
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Albendazole
Non-Proprietary Name
Albendazole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20181217
Marketing Category Name
ANDA
Application Number
ANDA208979
Manufacturer
Zydus Pharmaceuticals USA Inc.
Substance Name
ALBENDAZOLE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Anthelmintic [EPC], Cytochrome P450 1A Inducers [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-1021-8