First Nation Group, LLC

1 FDA products 1 active ingredients HUMAN PRESCRIPTION DRUG

First Nation Group, LLC is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human prescription drug products.

About First Nation Group, LLC

First Nation Group, LLC is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by DIVALPROEX SODIUM. Most of these labels are human prescription drug products. Labelling across this portfolio most often references: adjunctive therapy, absence seizures, divalproex sodium, delayed-release capsules, complex partial, multiple seizure, failed provide, adequate symptom. 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
DIVALPROEX SODIUM 1

Dosage forms and routes

Dosage formProductsRouteProducts
— — ORAL 1
— — — —
— — — —
— — — —
— — — —
— — — —

FDA drug products from First Nation Group, LLC

Brand nameGenericTypeRoute
divalproex sodium DIVALPROEX SODIUM HUMAN PRESCRIPTION DRUG ORAL

Frequently asked questions

How many FDA drug products does First Nation Group, LLC make?
1 FDA drug label records name First Nation Group, LLC as the manufacturer, covering 1 distinct active ingredients.

What active ingredients does First Nation Group, LLC produce?
The most frequent active ingredients in this portfolio are DIVALPROEX SODIUM.

Are First Nation Group, LLC 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.