NDC 23155-018
tetracycline hydrochloride 500 mg capsule
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Recalls
- Mar 23, 2020 · Class I · Avet Pharmaceuticals, Inc.
Failed Dissolution Specifications: Out of specification result during long term testing in Tetracycline HCl capsules.
Lots: Lot #s: G190609, G190610, G190611, Exp Jun 2022: L191027, L191028, Exp Nov 2022: K190953, K190952, Exp Oct 2022 - Mar 23, 2020 · Class I · Avet Pharmaceuticals, Inc.
Failed Dissolution Specifications: Out of specification result during long term testing in Tetracycline HCl capsules.
Lots: Lot # H190666, Exp JUL 2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Tetracycline: every company that makes it
- Form
- capsule, oral
- Strength
- 500 mg
- Approval
- NDA NDA050278
- On the market since
- Sep 15, 2024
- Package NDCs
23155-018-01- Official label
- DailyMed (National Library of Medicine), updated Mar 18, 2025
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