Package 70518-2970-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2970-1
Digits Only 7051829701
Product NDC 70518-2970
Product ID 70518-2970_4aba78bb-c18c-ab04-e063-6294a90a281d
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2970-1)

Marketing

Marketing Status
Marketed Since 2024-01-19
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": "4aba78bb-c18c-ab04-e063-6294a90a281d", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["e877a425-2b7f-4e43-a1f9-24019cbf9685"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2970-1)", "package_ndc": "70518-2970-1", "marketing_start_date": "20240119"}], "brand_name": "Gabapentin", "product_id": "70518-2970_4aba78bb-c18c-ab04-e063-6294a90a281d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2970", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20201216", "listing_expiration_date": "20271231"}