Losartan Potassium — manufacturers, supply & price · Pillstats

Who makes it34 active · 0 exited

US labelers as registered with FDA. Repackagers relabel another company's product; share* is of listed packages, not sales.

Labeler	Type	Packages	Status
Bryant Ranch Prepack	repackager	71	SUPPLYING
Proficient Rx LP	unknown	32	SUPPLYING
Preferred Pharmaceuticals, Inc.	unknown	26	SUPPLYING
A-S Medication Solutions	unknown	24	SUPPLYING
Alembic Pharmaceuticals Limited	unknown	24	SUPPLYING
Aphena Pharma Solutions - Tennessee, LLC	unknown	21	SUPPLYING
REMEDYREPACK INC.	repackager	17	SUPPLYING
NuCare Pharmaceuticals,Inc.	unknown	16	SUPPLYING
Zydus Lifesciences Limited	unknown	15	SUPPLYING
Zydus Pharmaceuticals USA Inc.	unknown	15	SUPPLYING
Camber Pharmaceuticals, Inc.	unknown	15	SUPPLYING
PD-Rx Pharmaceuticals, Inc.	unknown	14	SUPPLYING
Macleods Pharmaceuticals Limited	unknown	12	SUPPLYING
SOLCO HEALTHCARE US, LLC	unknown	11	SUPPLYING
Direct_Rx	unknown	9	SUPPLYING

+ 19 more labelers

Regulatory & supply eventsFDA · US

Shortages, recalls, and registration changes attached to this drug concept.

Jun 26, 2023
RECALLRecall (Class II): Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sci…
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet. — Recalling firm: Strides Pharma Inc. — Nationwide in the USA.
Jun 6, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles, Rx Only, Marketed and Packaged By: PD-Rx Pharmaceuticals, I…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: PD-Rx Pharmaceuticals, Inc. — Nationwide
Jun 6, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: PD-Rx Pharmaceuticals, Inc. — Nationwide
Jun 6, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP 25 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: PD-Rx Pharmaceuticals, Inc. — Nationwide
May 18, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP, 100 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: Strides Pharma Inc. — Nationwide
May 18, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP 25 mg, Rx only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101,…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: Strides Pharma Inc. — Nationwide
May 18, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP, 50 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101,…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: Strides Pharma Inc. — Nationwide
Apr 15, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottles (NDC # 33342-045-07), b) 90-count bottles (NDC # 33342-045-…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: Macleods Pharma Usa Inc — Product was distributed nationwide.
Apr 15, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP, 100 mg, a) 30-count bottles (NDC # 33342-046-07), b) 90-count bottles (NDC # 33342-046…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: Macleods Pharma Usa Inc — Product was distributed nationwide.
Apr 15, 2022
RECALLRecall (Class II): Losartan Potassium Tablets, USP, 25 mg, a) 90-count bottles (NDC # 33342-044-10), b) 1000-count bottles (NDC # 33342-04…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits — Recalling firm: Macleods Pharma Usa Inc — Product was distributed nationwide.
Jun 20, 2019
RECALLRecall (Class II): Losartan Potassium Tablets, USP 50 mg 90 tablets Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 0853…
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products. — Recalling firm: Macleods Pharma Usa Inc — Nationwide
Jun 20, 2019
RECALLRecall (Class II): Losartan Potassium Tablets 50 mg 1000 Tablets, USP Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 0…
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products. — Recalling firm: Macleods Pharma Usa Inc — Nationwide
Mar 8, 2019
RECALLRecall (Class II): Losartan Potassium USP, 50 mg, RX Only, Pkg By PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 60 Tablet…
CGMP deviation: Product found to contain trace amounts of NMBA — Recalling firm: PD-Rx Pharmaceuticals, Inc. — AK, AZ, CA, CO, FL, KY, MA, MI, MN, NC, OH, OR, WI, WY
Feb 28, 2019
RECALLRecall (Class II): Losartan Potassium Tablets USP, 25 mg, Rx only, a) 90 count (NDC 31722-700-90), b) 500 count (NDC 31722-700-05) and c) …
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient — Recalling firm: Camber Pharmaceuticals Inc — Nationwide
Feb 28, 2019
RECALLRecall (Class II): Losartan Potassium Tablets USP, 50 mg, Rx only, a) 30 count (NDC 31722-701-30), b) 90 count (NDC 31722-701-90), c) 1000…
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient — Recalling firm: Camber Pharmaceuticals Inc — Nationwide
Feb 28, 2019
RECALLRecall (Class II): Losartan Potassium Tablets USP, 100 mg, Rx only, a) 30 count (NDC 31722-702-30), b) 90 count (NDC 31722-702-30), c) 100…
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient — Recalling firm: Camber Pharmaceuticals Inc — Nationwide
Sep 22, 2014
RECALLRecall (Class II): LOSARTAN POTASSIUM TABLETS USP, 25 mg, 1000 Tablet Bottles, Rx Only. Manufactured by: Micro Labs Limited, Goa-403 722, …
Failed Content Uniformity Specifications; Dry mix failed blend uniformity. — Recalling firm: Micro Labs Usa, Inc S — U.S. Including: New York

Losartan Potassium

US acquisition costNADAC · per unit

Medicaid dispensing volumeSDUD · per quarter

Who makes it34 active · 0 exited

Regulatory & supply eventsFDA · US