Package 50090-7269-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7269-0
Digits Only 5009072690
Product NDC 50090-7269
Product ID 50090-7269_ec8bdb92-9ffd-429b-856a-002a1b7fc19d
Description

90 TABLET, COATED in 1 BOTTLE (50090-7269-0)

Marketing

Marketing Status
Marketed Since 2024-10-08
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ec8bdb92-9ffd-429b-856a-002a1b7fc19d", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["081fd1de-acaa-4685-a053-4959d77b17e9"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-7269-0)", "package_ndc": "50090-7269-0", "marketing_start_date": "20241008"}], "brand_name": "Gabapentin", "product_id": "50090-7269_ec8bdb92-9ffd-429b-856a-002a1b7fc19d", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7269", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20271231"}