Drug application

NEOPASALATE (AMINOSALICYLATE SODIUM, AMINOSALICYLIC ACID)

Drugs@FDA ANDA 080059 · MEDPOINTE PHARM HLC

Key facts

Drug name NEOPASALATE
Active ingredients AMINOSALICYLATE SODIUM, AMINOSALICYLIC ACID
Application type ANDA
Application number 080059
Company MEDPOINTE PHARM HLC
Dosage forms TABLET, ORAL
Strength 846MG;112MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date Aug 12, 1975

At a glance

  • 1–9 Submissions
  • None Label versions
  • 1–9 Products
  • None Therapeutic equivalents

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Drugs@FDA applications

Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.

Source: U.S. Food and Drug Administration (FDA), Drugs@FDA

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