Package 60760-987-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 60760-987-90
Digits Only 6076098790
Product NDC 60760-987
Product ID 60760-987_07f08a40-e514-e778-e063-6294a90ae300
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-987-90)

Marketing

Marketing Status
Marketed Since 2023-10-06
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": "07f08a40-e514-e778-e063-6294a90ae300", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["07f07d15-ee91-8c2a-e063-6394a90a4624"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-987-90)", "package_ndc": "60760-987-90", "marketing_start_date": "20231006"}], "brand_name": "GABAPENTIN", "product_id": "60760-987_07f08a40-e514-e778-e063-6294a90ae300", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60760-987", "generic_name": "Gabapentin", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA214957", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}