NDC 63629-8815

Glatopa

Glatiramer Acetate

Glatopa is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Glatiramer Acetate.

• Product ID: 63629-8815_66ac278d-f24d-4cb5-9300-065188970169
• NDC: 63629-8815
• Product Type: Human Prescription Drug
• Proprietary Name: Glatopa
• Generic Name: Glatiramer Acetate
• Dosage Form: Injection, Solution
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 2015-06-18
• Marketing Category: ANDA /
• Application Number: ANDA090218
• Labeler Name: Bryant Ranch Prepack
• Substance Name: GLATIRAMER ACETATE
• Active Ingredient Strength: 20 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 63629-8815-1

30 BLISTER PACK in 1 CARTON (63629-8815-1) > 1 SYRINGE, GLASS in 1 BLISTER PACK > 1 mL in 1 SYRINGE, GLASS

• Marketing Start Date: 2021-09-10
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Glatopa" or generic name "Glatiramer Acetate"

NDC	Brand Name	Generic Name
0781-3234	Glatopa	Glatiramer Acetate
0781-3250	Glatopa	Glatiramer Acetate
63629-8815	Glatopa	Glatiramer Acetate
63629-8816	Glatopa	Glatiramer Acetate
68546-317	Copaxone	Glatiramer Acetate
68546-325	Copaxone	Glatiramer Acetate
0378-6960	Glatiramer Acetate	glatiramer acetate