Package 50090-7675-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7675-0
Digits Only 5009076750
Product NDC 50090-7675
Description

90 CAPSULE in 1 BOTTLE (50090-7675-0)

Marketing

Marketing Status
Marketed Since 2025-10-08
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": "499031e6-132b-4dab-a527-53ba561f5768", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["54c09aa5-6724-480a-a115-c88484e39e93"], "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 (50090-7675-0)", "package_ndc": "50090-7675-0", "marketing_start_date": "20251008"}], "brand_name": "Gabapentin", "product_id": "50090-7675_499031e6-132b-4dab-a527-53ba561f5768", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7675", "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": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20160218", "listing_expiration_date": "20271231"}