Package 71335-1041-2

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 71335-1041-2
Digits Only 7133510412
Product NDC 71335-1041
Description

18 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2)

Marketing

Marketing Status
Marketed Since 2024-04-02
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": "02a2ff55-579a-4049-a4f4-a9373b720d4e", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["b4954172-5439-48fd-8348-8a2e0d2fee62"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1041-1)", "package_ndc": "71335-1041-1", "marketing_start_date": "20190129"}, {"sample": false, "description": "18 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2)", "package_ndc": "71335-1041-2", "marketing_start_date": "20240402"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-1041-3)", "package_ndc": "71335-1041-3", "marketing_start_date": "20240402"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1041-4)", "package_ndc": "71335-1041-4", "marketing_start_date": "20200428"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5)", "package_ndc": "71335-1041-5", "marketing_start_date": "20190408"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6)", "package_ndc": "71335-1041-6", "marketing_start_date": "20181227"}], "brand_name": "Gabapentin", "product_id": "71335-1041_02a2ff55-579a-4049-a4f4-a9373b720d4e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-1041", "generic_name": "GABAPENTIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}