Package 70518-2356-2

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2356-2
Digits Only 7051823562
Product NDC 70518-2356
Description

120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2356-2)

Marketing

Marketing Status
Marketed Since 2020-05-13
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a042552-afa0-b1d8-e063-6294a90abfad", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["5a78ab50-993d-4857-be10-be665e02b353"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2356-0)", "package_ndc": "70518-2356-0", "marketing_start_date": "20191009"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2356-1)", "package_ndc": "70518-2356-1", "marketing_start_date": "20191021"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2356-2)", "package_ndc": "70518-2356-2", "marketing_start_date": "20200513"}], "brand_name": "Gabapentin", "product_id": "70518-2356_4a042552-afa0-b1d8-e063-6294a90abfad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2356", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20271231"}