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Ranitidine

RANITIDINE HYDROCHLORIDE

Active ingredient 3 prescription 2 over-the-counter 9 with labelling

Overview

Source: NDC Directory

Ingredient name

RANITIDINE HYDROCHLORIDE

Base moiety

RANITIDINE

RxNorm CUI

198191

UNII

BK76465IHM

Medication products

Brand names

Dosage forms

FAERS reports

118,947 · not a risk measure

Products containing this ingredient

Source: NDC Directory 7 products

Ranitidine Tablet, Coated
OTC ANDA 1 recall 1 NDC
Ranitidine Hydrochloride Powder
8 NDC
Ranitidine Hydrochloride Form II Powder
1 NDC
ACID REDUCER Famotidine · Tablet, Film Coated
OTC ANDA 11 NDC
Ranitidine Tablet
Rx ANDA TE AB 4 recalls 7 NDC
Ranitidine Capsule
Rx ANDA 2 NDC
Ranitidine Hydrochloride Capsule
Rx ANDA TE AB 2 recalls 2 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	2	Ranitidine Hydrochloride, Ranitidine Hydrochloride Form II
Capsule	2	Ranitidine, Ranitidine Hydrochloride
TABLET, Coated	1	Ranitidine
TABLET, Film Coated	1	ACID REDUCER
Tablet	1	Ranitidine

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