Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
Reported: October 17, 2018 Initiated: September 20, 2018 #D-0010-2019
Product Description
Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
Reason for Recall
CGMP Deviations; rejected product was used to manufacture final bulk lot
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 7777 bottles
- Distribution
- Nationwide
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2. Recalled by Pfizer Inc.. Units affected: 7777 bottles.
Why was this product recalled? ▼
CGMP Deviations; rejected product was used to manufacture final bulk lot
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 17, 2018. Severity: Moderate. Recall number: D-0010-2019.
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