Labetalol — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

LABETALOL HYDROCHLORIDE

Base moiety

LABETALOL

RxNorm CUI

896758

UNII

1GEV3BAW9J

Medication products

10

Brand names

5

Dosage forms

6

FAERS reports

13,250 · not a risk measure

Products containing this ingredient

Source: NDC Directory 10 products

LABETALOL HCl Injection
Rx ANDA TE AP 1 NDC
Labetalol HCL Labetalol Hydrochloride · Tablet, Film Coated
Rx ANDA TE AB 1 NDC
Labetalol HCl in Dextrose Labetalol Hydrochloride · Injection
Rx NDA 1 NDC
Labetalol Hydrochloride Powder
15 NDC
Labetalol Hydrochloride Aerosol
3 NDC
Labetalol HCl in Sodium Chloride Labetalol Hydrochloride · Injection
Rx NDA 3 NDC
Labetalol Hydrochloride Injection, Solution
Rx ANDA TE AP 3 recalls 14 NDC
Labetalol Hydrochloride Tablet, Film Coated
Rx ANDA TE AB 97 NDC
Labetalol Hydrochloride Injection
Rx ANDA TE AP 10 NDC
Labetalol Hydrochloride Tablet
Rx ANDA TE AB 17 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
Injection	4	LABETALOL HCl, Labetalol HCl in Dextrose, Labetalol HCl in Sodium Chloride, Labetalol Hydrochloride
TABLET, Film Coated	2	Labetalol HCL, Labetalol Hydrochloride
Powder	1	Labetalol Hydrochloride
Aerosol	1	Labetalol Hydrochloride
INJECTION, Solution	1	Labetalol Hydrochloride
Tablet	1	Labetalol Hydrochloride

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