United States · FDA National Drug Code directory

Glatopa

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63629-8816_d1f6c590-1315-4499-9fcd-75ff92dcc5c4
Product NDC
63629-8816
Form
INJECTION, SOLUTION
Composition / generic term
Glatiramer Acetate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20180212
Source listing expiry
20261231

Source-listed ingredients

  • GLATIRAMER ACETATE — 40 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 BLISTER PACK in 1 CARTON (63629-8816-1) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS · 63629-8816-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →