Package 72189-384-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72189-384-90
Digits Only 7218938490
Product NDC 72189-384
Product ID 72189-384_2c4cc298-5b75-73fe-e063-6394a90a2ff7
Description

90 CAPSULE in 1 BOTTLE (72189-384-90)

Marketing

Marketing Status
Marketed Since 2022-09-19
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": "2c4cc298-5b75-73fe-e063-6394a90a2ff7", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["e90d2e3d-ec86-7d1d-e053-2995a90a9167"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-384-90)", "package_ndc": "72189-384-90", "marketing_start_date": "20220919"}], "brand_name": "Gabapentin", "product_id": "72189-384_2c4cc298-5b75-73fe-e063-6394a90a2ff7", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-384", "generic_name": "Gabapentin", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA213603", "marketing_category": "ANDA", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}