Sciegen Pharmaceuticals Inc: 6 recalls on record
Recalls filed with 1 agency: FDA (6).
First recall on record: November 28, 2018. Most recent: March 8, 2023.
Risk classification: Class II: 5 · Class III: 1
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| March 8, 2023 | FDA | Gabapentin Tablets, USP 600 mg, 500 tablets per bottle, RX Only, Manufactured by ScieGen …D-0354-2023 | D-0354-2023 |
| November 28, 2018 | FDA | Westminister Irbesartan Tablets, USP, 150 mg, (a) 30-count bottle (NDC 69367-120-01), (b)…D-0268-2019 | D-0268-2019 |
| November 28, 2018 | FDA | GSMS Irbesartan Tablets, USP, 300 mg,(a) 30-count bottle (NDC 60429-642-30), (b) 90-count…D-0272-2019 | D-0272-2019 |
| November 28, 2018 | FDA | GSMS Irbesartan Tablets, USP, 75 mg, 30-count bottle, Rx Only, Manufactured by ScieGen Ph…D-0270-2019 | D-0270-2019 |
| November 28, 2018 | FDA | Westminister Irbesartan Tablets, USP, 75 mg (a) 30-count bottle (NDC 69367-119-01), (b) 9…D-0267-2019 | D-0267-2019 |
| November 28, 2018 | FDA | GSMS Irbesartan Tablets, USP, 150 mg, (a) 30-count bottle (NDC 60429-641-30), (b) 90-coun…D-0271-2019 | D-0271-2019 |
Questions about this company
- How many recalls does Sciegen Pharmaceuticals Inc have?
- Recalert has 6 U.S. recalls on record for Sciegen Pharmaceuticals Inc, published between November 28, 2018 and March 8, 2023.
- What was the most recent Sciegen Pharmaceuticals Inc recall?
- FDA recall D-0354-2023, published March 8, 2023: Gabapentin Tablets, USP 600 mg, 500 tablets per bottle, RX Only, Manufactured by ScieGen Pharmaceuticals Inc., Hauppauge, NY 11788, NDC: 50228-177-05.
- Which agencies have handled Sciegen Pharmaceuticals Inc recalls?
- Sciegen Pharmaceuticals Inc appears as the recalling firm in recalls from: FDA (6).
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