NDC 0404-9810

Adrenalin 1 mg per 1 mL injection

On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from ENDO USA, Inc.'s NDC 42023-159.

Where the pills inside were made

Factory	Where	Role	Last FDA inspection
Par Health USA, LLC	Rochester, MI, United States	Makes it	Serious problems, FDA actionOct 20, 2025 · 13 inspections, 1 with FDA action
Par Sterile Products LLC	Parsippany, New Jersey, United States	Makes it	No problems foundMar 11, 2014 · 2 inspections

Jan 17, 2024 · Class II · Henry Schein Inc. and Glove Club HSI Gloves Inc.
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Lots: Original Lot # 64103, exp. date 11/24 Repackaged Lot # 39747, exp. date 01/26
Jan 17, 2024 · Class II · Henry Schein Inc. and Glove Club HSI Gloves Inc.
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Lots: Original Lot # 64103, exp. date 11/24 Repackaged Lot # 39747, exp. date 01/26
Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.

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

Generic drug: Epinephrine: every company that makes it
Form: injection, intramuscular; intravenous; subcutaneous
Strength: 1 mg per 1 mL
Approval: NDA NDA204200
On the market since: Jan 7, 2022
Package NDCs: 0404-9810-01
Official label: DailyMed (National Library of Medicine), updated Oct 22, 2026

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