NDC 0703-4502
Metoclopramide 5 mg per 1 mL injection, solution
On the label: Teva Parenteral Medicines, Inc..
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 Teva Parenteral Medicines, Inc. names for other drugs.
Recalls
- Jul 29, 2021 · Class II · Teva Pharmaceuticals USA
Lack of Assurance of Sterility
Lots: Lot #: 31326043B, exp. date 10/2021; 31326138B, exp. date 11/2021 31329399B, 31329539B, exp. date 08/2023; 31329599B, exp. date 09/2023 - Apr 26, 2021 · Class II · Teva Pharmaceuticals USA
Lack of Assurance of Sterility
Lots: Lot # 31325459B, exp. date 08/2021 - Feb 15, 2021 · Class II · Teva Pharmaceuticals USA
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Lots: Lot # 31325335B, exp. date 07/2021 - Feb 10, 2021 · Class II · Teva Pharmaceuticals USA
Lack of Assurance of Sterility: manufacturing areas for the recalled products exceeded acceptance levels for microbial recovery leading to a lack of sterility assurance for these sterile injectable products.
Lots: Lot # 31325042B, exp. date 06/2021 31325336B, exp. date 07/2021 31326042B, exp. date 10/2021 31326137B, exp. date 11/2021 31326230B, exp. date 12/2021 31323816B, exp. date 02/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Metoclopramide: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA073135
- On the market since
- Dec 1, 1991
- Package NDCs
0703-4502-010703-4502-04- Official label
- DailyMed (National Library of Medicine), updated Apr 22, 2026
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