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"68382-914-84" National Drug Code (NDC)
Erlotinib 3 BLISTER PACK in 1 CARTON (68382-914-84) / 10 TABLET in 1 BLISTER PACK (68382-914-30)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-914-84
Package Description
3 BLISTER PACK in 1 CARTON (68382-914-84) / 10 TABLET in 1 BLISTER PACK (68382-914-30)
Product NDC
68382-914
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Erlotinib
Non-Proprietary Name
Erlotinib
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200430
Marketing Category Name
ANDA
Application Number
ANDA213065
Manufacturer
Zydus Pharmaceuticals USA Inc.
Substance Name
ERLOTINIB HYDROCHLORIDE
Strength
100
Strength Unit
mg/1
Pharmacy Classes
Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-914-84