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"70771-1522-7" National Drug Code (NDC)
Erlotinib 3 BLISTER PACK in 1 CARTON (70771-1522-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)
(Cadila Healthcare Limited)
NDC Code
70771-1522-7
Package Description
3 BLISTER PACK in 1 CARTON (70771-1522-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)
Product NDC
70771-1522
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Erlotinib
Non-Proprietary Name
Erlotinib
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200430
Marketing Category Name
ANDA
Application Number
ANDA213065
Manufacturer
Cadila Healthcare Limited
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/70771-1522-7