Drug recall
RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals…
FDA recall event 79367 · Class II · Mckesson Packaging Services
Key facts
| Event ID | 79367 |
|---|---|
| Recall numbers | D-0914-2018 |
| Recalling firm | Mckesson Packaging Services |
| Product type | Drugs |
| Products | RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Stability Specifications |
| Initiation date | Feb 26, 2018 |
| Report date | Mar 14, 2018 |
| Termination date | Sep 15, 2020 |
| City | Concord |
| State | NC |
| Country | United States |
| FEI number | 3000206187 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: