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Active Shortage Injection Anesthesia

Bupivacaine Hydrochloride, Epinephrine Bitartrate Injection

Brand: BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE

This drug is currently listed as in shortage by the FDA. Affected manufacturer: Hospira, Inc., a Pfizer Company.

Active FDA Drug Shortage

Contact your pharmacist if you are affected. They can check availability from other manufacturers or suggest alternatives.

Shortage Details

Generic Name
Bupivacaine Hydrochloride, Epinephrine Bitartrate Injection
Manufacturer
Hospira, Inc., a Pfizer Company
Dosage Form
Injection
Presentation
Bupivacaine Hydrochloride and Epinephrine, Injection, 125 mg/50 mL (2.5 mg/mL) (NDC 0409-9043-01)
Package NDC
0409-9043-01

Status & Timeline

Status
Active Shortage
Availability
Unavailable
First Reported
Feb 20, 2018
Last Updated
Mar 13, 2026
Therapeutic Category
Anesthesia

Shortage Reason

Next Delivery and Estimated Recovery: December 2028; Shortage per Manufacturer: Manufacturing Delay

Nearby — Other Bupivacaine Shortage Records

Frequently Asked Questions

Why is Bupivacaine in shortage?
According to FDA data: Next Delivery and Estimated Recovery: December 2028; Shortage per Manufacturer: Manufacturing Delay
What can I do if my medication is in shortage?
Contact your pharmacist — they can check availability across suppliers or suggest an equivalent from a different manufacturer. Your prescriber may also recommend a therapeutic substitute from the same drug class.
How often is this data updated?
Shortage data comes from the FDA Drug Shortages Database via openFDA. The database is updated regularly as manufacturers report changes to the FDA.

What This Bupivacaine Shortage Record Means

The FDA Drug Shortages database lists this record for Bupivacaine Hydrochloride, Epinephrine Bitartrate Injection (brand: BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE) from Hospira, Inc., a Pfizer Company with a current status of Active Shortage. The affected dosage form is Injection, presented as Bupivacaine Hydrochloride and Epinephrine, Injection, 125 mg/50 mL (2.5 mg/mL) (NDC 0409-9043-01). Shortages are tracked at the manufacturer and presentation level — other manufacturers or formulations of the same generic may remain available, which is why pharmacists often can source a working substitute even when one record is flagged.

This shortage was first reported on Feb 20, 2018 and was last updated Mar 13, 2026. The FDA cites the following reason: Next Delivery and Estimated Recovery: December 2028; Shortage per Manufacturer: Manufacturing Delay. There are 6 other current records in this database covering the same generic, which gives a fuller picture of how disruption is playing out across manufacturers and dosage forms.

A shortage listing is a supply-side signal, not a patient-level instruction. Access can vary dramatically by pharmacy, region, hospital system, and insurance formulary — local pharmacists have real-time visibility that a national database cannot provide. Therapeutic substitutes often exist in the same class, but switching decisions belong with your prescriber, who weighs efficacy, dosing conversion, interaction profile, and personal history. This page summarizes public FDA data for educational reference only and is not medical advice. If your medication is affected, contact your pharmacist and prescriber to plan an appropriate response.

Disclaimer: This information comes from the FDA Drug Shortages Database and is for educational purposes only. It is not medical advice. Do not stop or change any medication without consulting your healthcare provider or pharmacist. Shortage status can change rapidly — always verify current availability with your pharmacist.