Package 60760-066-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 60760-066-90
Digits Only 6076006690
Product NDC 60760-066
Product ID 60760-066_35d33092-9ebd-3906-e063-6294a90ab7d2
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-066-90)

Marketing

Marketing Status
Marketed Since 2025-05-15
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": "35d33092-9ebd-3906-e063-6294a90ab7d2", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["7d3fc163-25f0-2c61-e053-2991aa0a76e9"], "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, FILM COATED in 1 BOTTLE, PLASTIC (60760-066-90)", "package_ndc": "60760-066-90", "marketing_start_date": "20250515"}], "brand_name": "Gabapentin", "product_id": "60760-066_35d33092-9ebd-3906-e063-6294a90ab7d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60760-066", "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": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20181217", "listing_expiration_date": "20261231"}