NDC 70710-1549-2 - GLATIRAMER ACETATE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70710-1549
Requested NDC
70710-1549-2
Package NDCs from labels
70710-1549-2, 70710-1549-6
Manufacturer
Zydus Pharmaceuticals USA Inc. | Italfarmaco SpA
Effective date
2026-08-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
GLATIRAMER ACETATE - Zydus Pharmaceuticals USA Inc. | Italfarmaco SpAZydus Pharmaceuticals USA Inc. | Italfarmaco SpA2026-08-19HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1549-2GLATIRAMER ACETATE1 mL in 1 SYRINGEINJECTION, SOLUTION11
70710-1549-6GLATIRAMER ACETATE1 in 1 BLISTER PACKINJECTION, SOLUTION11
70710-1549-6GLATIRAMER ACETATE12 in 1 CARTONINJECTION, SOLUTION121

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1549-2ML - Milliliter70710-1549da7489ef-9b00-4870-8735-adcfbd9c76d612025-12-16
70710-1549-6ML - Milliliter70710-1549770d7c39-0593-4480-ad88-6ae3c6bdf6a712025-12-16

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 2 · 23 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MANNITOLMANNITOLHF Acquisition Co LLC, DBA HealthFirst999ce711-2d5b-0d7d-e053-2995a90a26892024-01-27Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
MannitolMANNITOLB. Braun Medical Inc.d12cc802-b538-4065-a264-f474ff3b30432023-08-15Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
MannitolMANNITOLFresenius Kabi USA, LLCc395e13d-6ea1-4104-8b37-669cfb982f042023-03-16Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.