Erlotinib — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

ERLOTINIB HYDROCHLORIDE

Base moiety

ERLOTINIB

RxNorm CUI

603203

UNII

DA87705X9K

Medication products

8

Brand names

2

Dosage forms

4

FAERS reports

12,441 · not a risk measure

Products containing this ingredient

Source: NDC Directory 8 products

Erlotinib Powder
2 NDC
Erlotinib HCl Powder
3 NDC
Erlotinib Hydrochloride Powder
9 NDC
Erlotinib Hydrochloride Powder, for Suspension
1 NDC
Erlotinib Hydrochloride (Form-B) Powder
1 NDC
Erlotinib Tablet
Rx ANDA TE AB 3 NDC
Erlotinib Tablet, Film Coated
Rx ANDA TE AB 18 NDC
ERLOTINIB HYDROCHLORIDE Erlotinib Hydrochloride · Tablet, Film Coated
Rx ANDA TE AB 9 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	4	Erlotinib, Erlotinib HCl, Erlotinib Hydrochloride, Erlotinib Hydrochloride (Form-B)
TABLET, Film Coated	2	Erlotinib, ERLOTINIB HYDROCHLORIDE
POWDER, For Suspension	1	Erlotinib Hydrochloride
Tablet	1	Erlotinib

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals