Pharmaceutical companyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Pfizer. FDA records under its name, each linked to the record. See the Pfizer group view.
As of Nov 15, 2026, FDA's public records list Pfizer US Pharmaceuticals Group with 4 drug recalls. The most recent is a drug recall dated Apr 16, 2014: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distr….
| Apr 16, 2014 | Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, Inc., NDC 0008-121Class II · Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq (desvenlafaxine) extended release tablets becaus | Drug recalls |
| Mar 6, 2014 | Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC 0008-0836-21) UPC 3 0008-08Class I · Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a sing | Drug recalls |
| Feb 26, 2014 | Advil PM Caplets, (Ibuprofen, 200 mg /Diphenhydramine citrate, 38 mg) 120 count bottle, OTC, Pfizer, Madison, NJ 07940 USA. NDC 0573-0164-43Class III · Subpotent Drug: This lot is being recalled because of out-of-specification test results for Diphenhydramine citrate. | Drug recalls |
| Sep 4, 2013 | Aldactone (spironolactone) tablets, USP, 100 mg, 100-count bottles, Rx only, Distributed by G.D. Searle, Division of Pfizer Inc, NY, NY 100Class II · Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in d | Drug recalls |
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