BluePoint Laboratories Inc.

1 FDA products 1 active ingredients HUMAN PRESCRIPTION DRUG

BluePoint Laboratories Inc. is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human prescription drug products.

About BluePoint Laboratories Inc.

BluePoint Laboratories Inc. is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by LABETALOL HYDROCHLORIDE. Most of these labels are human prescription drug products. Labelling across this portfolio most often references: labetalol hydrochloride, tablets usp, management hypertension, alone combination, antihypertensive agents, especially thiazide, loop diuretics. Use the table below to identify a specific product, then open it for full indications, dosage and warnings as filed with the FDA.

Active ingredients in this portfolio

Active ingredientProducts
LABETALOL HYDROCHLORIDE 1

Dosage forms and routes

Dosage formProductsRouteProducts
— — ORAL 1
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FDA drug products from BluePoint Laboratories Inc.

Brand nameGenericTypeRoute
Labetalol Hydrochloride LABETALOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG ORAL

Frequently asked questions

How many FDA drug products does BluePoint Laboratories Inc. make?
1 FDA drug label records name BluePoint Laboratories Inc. as the manufacturer, covering 1 distinct active ingredients.

What active ingredients does BluePoint Laboratories Inc. produce?
The most frequent active ingredients in this portfolio are LABETALOL HYDROCHLORIDE.

Are BluePoint Laboratories Inc. products prescription or over-the-counter?
The largest share of this company’s labels are human prescription drug products; check each product page for its own marketing status.

Does this page list prices or where to buy?
No. This is a labelling reference built from FDA data. It does not sell, price or recommend any medicine.

Labelling data reproduced from FDA Structured Product Labelling for identification only. This site does not sell, price or recommend any medicine.