What is NDC 48951-2118?
The NDC code 48951-2118 is assigned by the FDA to the product Berberis Oxalis which is a human over the counter drug product labeled by Uriel Pharmacy Inc.. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 48951-2118-1 10 ampule in 1 box / 1 ml in 1 ampule. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.
What are the uses for Berberis Oxalis?
NDC Code 48951-2118-1
Package Description: 10 AMPULE in 1 BOX / 1 mL in 1 AMPULE
Berberis Oxalis Product Label
FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
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