Package 70518-2919-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2919-1
Digits Only 7051829191
Product NDC 70518-2919
Product ID 70518-2919_4ab8d0dd-0947-3d29-e063-6294a90ab17a
Description

30 CAPSULE in 1 BLISTER PACK (70518-2919-1)

Marketing

Marketing Status
Marketed Since 2025-08-14
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

GABAPENTIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4ab8d0dd-0947-3d29-e063-6294a90ab17a", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310432"], "spl_set_id": ["915cee37-536c-4761-bdb9-b96c7ee0f956"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-2919-1)", "package_ndc": "70518-2919-1", "marketing_start_date": "20250814"}], "brand_name": "GABAPENTIN", "product_id": "70518-2919_4ab8d0dd-0947-3d29-e063-6294a90ab17a", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2919", "generic_name": "GABAPENTIN", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA090007", "marketing_category": "ANDA", "marketing_start_date": "20201023", "listing_expiration_date": "20271231"}