Package 50090-6718-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-6718-0
Digits Only 5009067180
Product NDC 50090-6718
Description

90 CAPSULE in 1 BOTTLE (50090-6718-0)

Marketing

Marketing Status
Marketed Since 2023-10-05
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9ab3c803-abb0-41c6-8e8f-ec674e23aa1d", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["3dbd447f-4791-4c62-86b4-6f7928862785"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6718-0)", "package_ndc": "50090-6718-0", "marketing_start_date": "20231005"}], "brand_name": "Gabapentin", "product_id": "50090-6718_9ab3c803-abb0-41c6-8e8f-ec674e23aa1d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-6718", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA078787", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20271231"}