Package 62756-139-04

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 62756-139-04
Digits Only 6275613904
Product NDC 62756-139
Product ID 62756-139_aff50a15-df39-495f-a145-0ba59660eed8
Description

1000 CAPSULE in 1 BOTTLE (62756-139-04)

Marketing

Marketing Status
Marketed Since 2022-02-01
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": "aff50a15-df39-495f-a145-0ba59660eed8", "openfda": {"nui": ["N0000008486"], "upc": ["0362756204010", "0362756202016", "0362756138025", "0362756137028", "0362756139022"], "unii": ["6CW7F3G59X"], "spl_set_id": ["c9a05f0c-b5f0-422c-9d67-6d0efc921a74"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOX, UNIT-DOSE (62756-139-01)", "package_ndc": "62756-139-01", "marketing_start_date": "20220201"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-139-02)", "package_ndc": "62756-139-02", "marketing_start_date": "20220201"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-139-03)", "package_ndc": "62756-139-03", "marketing_start_date": "20220201"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62756-139-04)", "package_ndc": "62756-139-04", "marketing_start_date": "20220201"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (62756-139-05)", "package_ndc": "62756-139-05", "marketing_start_date": "20220201"}], "brand_name": "gabapentin", "product_id": "62756-139_aff50a15-df39-495f-a145-0ba59660eed8", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "62756-139", "generic_name": "gabapentin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA077242", "marketing_category": "ANDA", "marketing_start_date": "20220201", "listing_expiration_date": "20261231"}