Package 69367-347-05

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 69367-347-05
Digits Only 6936734705
Product NDC 69367-347
Product ID 69367-347_3855844f-e123-4574-8d9b-76397d602744
Description

500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-347-05)

Marketing

Marketing Status
Marketed Since 2021-11-01
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": "3855844f-e123-4574-8d9b-76397d602744", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["2eec52a1-9016-46dd-8b4c-8dab1d0aeece"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-347-05)", "package_ndc": "69367-347-05", "marketing_start_date": "20211101"}], "brand_name": "Gabapentin", "product_id": "69367-347_3855844f-e123-4574-8d9b-76397d602744", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "69367-347", "generic_name": "Gabapentin", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}