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 Acella Pharmaceuticals, LLC names for other drugs.
Recalls
- Nov 14, 2022 · Class III · Acella Pharmaceuticals, LLC
Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.
Lots: Lot: E025A001 Exp. 07/2023 - Nov 14, 2022 · Class III · Acella Pharmaceuticals, LLC
Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.
Lots: Lot: E026A001 Exp. 06/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Phenytoin: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA040573
- On the market since
- Dec 1, 2021
- Package NDCs
42192-614-1042192-614-30- Official label
- DailyMed (National Library of Medicine), updated Sep 16, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?