Lupin Pharmaceuticals Inc.: 103 recalls on record

Recalls filed with 1 agency: FDA (103).

First recall on record: April 24, 2013. Most recent: September 2, 2026.

Risk classification: Class I: 4 · Class II: 69 · Class III: 30

Most recent recalls

DateAgencyProduct
March 27, 2019FDATestosterone Topical Solution, 30mg/1.5mL, 110mL bottles, Rx only, Manufactured for: Lupi…D-1010-2019
February 6, 2019FDACephalexin for Oral Suspension USP 250mg/5 mL, Rx Only Manufactured for: Lupin Pharmace…D-0423-2019
January 16, 2019FDACefdinir for Oral Suspension USP, 250mg/5mL, packaged in a) 60mL (NDC 68180-723-20), b)10…D-0376-2019
January 16, 2019FDACeftriaxone for Injection USP, 500 mg, packaged in a) one Single Use Vial (NDC 68180-622-…D-0356-2019
January 16, 2019FDACeftriaxone for Injection USP, 250 mg, packaged in a) one Single Use Vial (NDC 68180-611-…D-0355-2019
January 16, 2019FDACefdinir for Oral Suspension USP, 125mg/5mL, packaged in a) 60mL (NDC 68180-722-20), b)10…D-0375-2019
January 16, 2019FDACeftriaxone for Injection USP, 1 g, packaged in a) one Single Use Vial (NDC 68180-633-01)…D-0357-2019
October 31, 2018FDATestosterone Topical Solution, 30mg/1.5mL, 110mL bottles, Rx only, Manufactured for: Lupi…D-0087-2019
August 8, 2018FDAMoxifloxacin Ophthalmic Solution USP, 0.5%, 5 mL bottle, Rx only, Manufactured for: Lupi…D-1050-2018
May 30, 2018FDAMy Way (Levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5m…D-0837-2018
May 30, 2018FDAMy Way (levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5m…D-0838-2018
April 25, 2018FDALupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 6818…D-0684-2018
December 6, 2017FDADuloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured f…D-0097-2018
September 13, 2017FDAFamotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: …D-1127-2017
July 19, 2017FDAParoxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured …D-0974-2017
April 12, 2017FDAQuinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD …D-0650-2017
September 28, 2016FDALisinopril Tablets USP, 40 mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharm…D-1503-2016
September 28, 2016FDALisinopril Tablets USP, 30 mg, packaged in a) 500-count bottles (NDC 68180-516-02) and b)…D-1502-2016
July 6, 2016FDALisinopril & Hydrochlorothiazide Tables, USP 20mg/12.5mg, packaged in a)100-count bottles…D-1052-2016
June 8, 2016FDACeftriaxone for Injection USP, 2 g, Single Use Vial (NDC 68180-644-01) packaged in 10-cou…D-0954-2016
June 8, 2016FDACeftriaxone for Injection USP, 1 g, Single Use Vial (NDC 68180-633-01) packaged in 10-cou…D-0953-2016
June 8, 2016FDACeftriaxone for Injection USP, 500 mg, Single Use Vial, packaged in a) 1-count Vials per …D-0952-2016
April 9, 2014FDASuprax, Cefixime for Oral Suspension USP 500 mg/5 ml, 10mL (when reconstituted), Rx only,…D-1186-2014
April 9, 2014FDASuprax, Cefixime for Oral Suspension USP, 500 mg/5 ml, 20 mL (when reconstituted), Rx on…D-1187-2014
January 22, 2014FDAQuinapril Tablets USP, 10 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmace…D-409-2014

Questions about this company

How many recalls does Lupin Pharmaceuticals Inc. have?
Recalert has 103 U.S. recalls on record for Lupin Pharmaceuticals Inc., published between April 24, 2013 and September 2, 2026.
Which agencies have handled Lupin Pharmaceuticals Inc. recalls?
Lupin Pharmaceuticals Inc. appears as the recalling firm in recalls from: FDA (103).

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