Package 71335-2280-2
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
71335-2280-2
Digits Only
7133522802
Product NDC
71335-2280
Description
500 CAPSULE in 1 BOTTLE (71335-2280-2)
Marketing
Marketing Status
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": "fae067e5-38bb-499c-94a2-b0de781fd173", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["9efd0261-9fc9-4dc9-8cf3-9110157ddfc4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (71335-2280-1)", "package_ndc": "71335-2280-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (71335-2280-2)", "package_ndc": "71335-2280-2", "marketing_start_date": "20240403"}], "brand_name": "Gabapentin", "product_id": "71335-2280_fae067e5-38bb-499c-94a2-b0de781fd173", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2280", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA206943", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}