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"63304-096-11" National Drug Code (NDC)
Erlotinib 3 BLISTER PACK in 1 CARTON (63304-096-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
63304-096-11
Package Description
3 BLISTER PACK in 1 CARTON (63304-096-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31)
Product NDC
63304-096
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Erlotinib
Non-Proprietary Name
Erlotinib
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20191105
Marketing Category Name
ANDA
Application Number
ANDA210300
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
ERLOTINIB
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/63304-096-11