NDC 36000-372
Acetaminophen 10 mg per 1 mL injection, solution
On the label: Baxter Healthcare Corporation.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Baxter Healthcare Corporation names for other drugs.
Recalls
- Aug 20, 2025 · Class II · Baxter Healthcare Corporation
Discoloration
Lots: Lot #: 24A27G66, Exp 12/31/2025 - Aug 4, 2022 · Class II · Baxter Healthcare Corporation
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.
Lots: Lots: 20K19G64T1, Exp 10/31/2022; 21K23G65, 21K25G65, 21K26G65, 21K29G67, Exp 10/31/2023; 21L10G65, 21L13G66, 21L14G66, 21L15G65, Exp 11/30/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acetaminophen: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA214331
- On the market since
- May 21, 2025
- Package NDCs
36000-372-40- Official label
- DailyMed (National Library of Medicine), updated May 6, 2024
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