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Rx only · Injection, Solution · Intravenous

Norepinephrine Bitartrate

Norepinephrine Bitartrate

4 ACTIVE SUPPLIERS — US
openFDA · updated weekly
US12 NDCs
4 active makers
UKComing
soon
CAComing
soon
AUComing
soon
EUComing
soon
RxCUI (US)7512
US makers4 labelers
Packages12
DEA / ScheduleNone

Medicaid dispensing volumeSDUD · per quarter

Prescriptions dispensed under Medicaid (fee-for-service + managed care), summed nationally. The closest free proxy to sales volume — Medicaid only, not all-payer.

2054106158202025 Q12025 Q22025 Q32025 Q42026 Q1
263
Rx · 2026 Q1
35K
Units dispensed
-63%
Rx vs. year ago
5
Quarters · since 2025 Q1

Who makes it4 active · 0 exited

US labelers as registered with FDA. Repackagers relabel another company's product; share* is of listed packages, not sales.

LabelerTypePackagesStatus
Baxter Healthcare Corporationunknown6SUPPLYING
WG Critical Care, LLCunknown4SUPPLYING
Avenacy, LLCunknown1SUPPLYING
Sagent Pharmaceuticalsunknown1SUPPLYING

Regulatory & supply eventsFDA · US

Shortages, recalls, and registration changes attached to this drug concept.

  • Jan 23, 2024
    RECALLRecall (Class II): Norepinephrine Bitartrate in 5% Dextrose Injection, 8 mg/ 250 mL (32 mcg/mL), For Intravenous Infusion Only, 250 mL via…

    Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified the product strength as 8 mg / 250 mL. — Recalling firm: Baxter Healthcare Corporation — Nationwide in the USA