NDC 51662-1396

Bupivacaine Hydrochloride 5 mg per 1 mL injection, solution

On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-1163.

United States: 1India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Hospira, Inc.Rocky Mount, NC, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action
Pfizer Healthcare India Private LimitedAnakapalli, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 with FDA action

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Bupivacaine: every company that makes it
Form
injection, solution, perineural
Strength
5 mg per 1 mL
Approval
ANDA ANDA070597
On the market since
Oct 16, 2019
Package NDCs
51662-1396-1 51662-1396-2 51662-1396-3
Official label
DailyMed (National Library of Medicine), updated Jun 20, 2024

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