Package 70518-3708-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-3708-0
Digits Only 7051837080
Product NDC 70518-3708
Description

10 CUP, UNIT-DOSE in 1 BOX (70518-3708-0) / 10 mL in 1 CUP, UNIT-DOSE (70518-3708-1)

Marketing

Marketing Status
Marketed Since 2023-04-11
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f290872-8935-79f1-e063-6394a90a3e67", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["cfd8122f-8b23-42c1-97e8-43df98af88e0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 CUP, UNIT-DOSE in 1 BOX (70518-3708-0)  / 10 mL in 1 CUP, UNIT-DOSE (70518-3708-1)", "package_ndc": "70518-3708-0", "marketing_start_date": "20230411"}], "brand_name": "Gabapentin", "product_id": "70518-3708_3f290872-8935-79f1-e063-6394a90a3e67", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-3708", "generic_name": "gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA076403", "marketing_category": "ANDA", "marketing_start_date": "20230411", "listing_expiration_date": "20261231"}