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
December 20, 2023FDAPenicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Phar…D-0148-2024
August 9, 2023FDATydemy (drospirenone, ethinyl estradiol and levomefolate calcium tablets, 3 mg/0.03 mg/0.…D-1081-2023
July 19, 2023FDAAmlodipine Besylate Tablets, USP 10 mg, 1000-count bottles, Rx only, Manufactured for: Lu…D-0899-2023
February 1, 2023FDAClobetasol propionate Cream USP, 0.05%, 45 g tube, Rx only, Manufactured for: Lupin Pharm…D-0174-2023
January 18, 2023FDARifampin Capsules USP, 300 mg, 30-count bottle; Rx Only, Manufactured for: Lupin Pharmace…D-0100-2023
December 28, 2022FDAQuinapril Tablets USP, 40 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,…D-0088-2023
December 28, 2022FDAQuinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,…D-0089-2023
September 21, 2022FDALisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only, Manufactured for: Lupin Pharm…D-1536-2022
August 24, 2022FDARifampin Capsules, USP, 150 mg, 30 count HDPE bottles, Rx Only, Manufactured for Lupin Ph…D-1343-2022
June 22, 2022FDAZileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lu…D-1150-2022
May 25, 2022FDAGaviLyte -C (Polyethylene Glycol 3350, 240 g) and electrolytes for Oral Solution, USP wit…D-0875-2022
May 11, 2022FDALosartan Potassium Tablets USP, 100 mg, a) 90-count bottles (NDC# 68180-378-03), b) 1000…D-0840-2022
May 11, 2022FDALosartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/12.5 mg a) 30-count bottl…D-0843-2022
May 11, 2022FDALosartan Potassium and Hydrochlorothiazide Tablets USP, 50 mg/12.5 mg a) 30-count bottle…D-0841-2022
May 11, 2022FDALosartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/25 mg a) 30-count bottles…D-0842-2022
May 11, 2022FDALosartan Potassium Tablets USP, 25 mg, a) 90-count bottles (NDC# 68180-376-03), b) 1000-c…D-0838-2022
May 11, 2022FDALosartan Potassium Tablets USP, 50 mg, a) 90-count bottles (NDC# 68180-377-03), b) 1000-c…D-0839-2022
January 12, 2022FDAOxycodone Hydrochloride Tablets, USP C-II, 5 mg, 100 count bottles, Rx Only, Manufactured…D-0358-2022
January 12, 2022FDAGatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Li…D-0326-2022
December 8, 2021FDATydemy (drospirenone, ethinyl estradiol & levomefolate calcium tablets, 3 mg/0.03 mg/0.45…D-0264-2022
November 10, 2021FDAIrbesartan Tablets USP, 75 mg a) 30 count (NDC 68180-410-06) and b) 90 count (NDC 68180-…D-0086-2022
November 10, 2021FDAIrbesartan Tablets USP, 150 mg a) 30 count (NDC 68180-411-06) and b) 90 count (NDC 68180…D-0087-2022
November 10, 2021FDAIrbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-0…D-0090-2022
October 27, 2021FDAImipramine Pamoate Capsules 125 mg, 30-count bottle, Rx only, Manufactured for Lupin Phar…D-0027-2022
May 26, 2021FDACefixime for Oral Suspension USP 100 mg/5mL, 50mL HDPE bottles, Rx Only, Manufactured by:…D-0390-2021

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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