USFDA APPLICATION NUMBER - 21743 / DOSAGE - TABLET;ORAL - EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
ERLOTINIB HYDROCHLORIDE(UNII: DA87705X9K) (ERLOTINIB - UNII:J4T82NDH7E) | ERLOTINIB | 100mg |
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