NDC 70934-384
Metoclopramide 10 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-2203.
Where the pills inside were 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 Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Recalls
- Sep 29, 2026 · Class II · Teva Pharmaceuticals USA, Inc
Presence of Foreign Tablets/Capsules
Lots: Lot, expiry: [100 Tablets] Lots 8634085, 8635085, 8636085, exp 07/2027; [500 Tablets] Lot 8633085, exp 07/2027 - May 23, 2025 · Class II · Teva Pharmaceuticals USA, Inc
Presence of foreign tablets/capsules.
Lots: Lot#: 5420094, Exp 09/30/2027
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
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA070184
- On the market since
- Jun 3, 2019
- Package NDCs
70934-384-06- Official label
- DailyMed (National Library of Medicine), updated Dec 30, 2020
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