Laurus Labs Limited Products: Prescription Medications Section

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Efavirenz, Lamivudine and Tenofovir Disoproxil Fumarate

Efavirenz, lamivudine and tenofovir disoproxil fumarate tablets are indicated as a complete regimen for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in adult and…

Laurus Labs Limited21 May 2020

Emtricitabine and Tenofovir Disoproxil Fumarate

HIV-1 Treatment (1.1) Emtricitabine and tenofovir disoproxil fumarate tablets are a two-drug combination of emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF), both HIV-1…

Laurus Labs Limited31 December 2020

Fenofibrate

Fenofibrate tablets are peroxisome proliferator-activated receptor (PPAR) alpha agonist indicated as an adjunct to diet: To reduce elevated LDL-C. Total-C. TG and Apo B, and to increase…

Laurus Labs Limited20 August 2020

FENOFIBRIC ACID DELAYED-RELEASE (FENOFIBRIC ACID)

Fenofibric acid delayed-release capsules are peroxisome proliferator-activated receptor (PPAR) alpha agonist indicated as adjunctive therapy to diet to: Reduce TG in patients with severe…

Laurus Labs Limited31 May 2020

Hydroxychloroquine Sulfate

Malaria. Hydroxychloroquine sulfate tablets are indicated for the treatment of uncomplicated malaria due to P. falciparum. P. malariae. P. ovale, and P. vivax. Hydroxychloroquine sulfate…

Laurus Labs Limited4 September 2019

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FDA Medwatch

Nostrum Laboratories, Inc. Expands Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 750 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit
Sun, 24 Jan 2021. Nostrum Laboratories, Inc. is voluntarily recalling one lot of Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) to the consumer level. The Metformin HCl Extended Release Tablets, USP 750 mg (generic…
Boston Scientific Announces LOTUS Edge™ Aortic Valve System Voluntary Recall and Product Discontinuation
Sun, 10 Jan 2021. Boston Scientific Corporation (NYSE: BSX) has announced it has initiated a global, voluntary recall of all unused inventory of the LOTUS Edge™ Aortic Valve System due to complexities associated with the product delivery system. The voluntary…

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As a leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. RxDrugLabels.com provides the full prescription-only subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.