Package 31722-069-47

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 31722-069-47
Digits Only 3172206947
Product NDC 31722-069
Description

1 BOTTLE in 1 CARTON (31722-069-47) / 470 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-01-17
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45c076af-c121-6962-e063-6394a90aaad1", "openfda": {"nui": ["N0000008486"], "upc": ["0331722069472"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["b86c81d9-9a4a-4847-be18-520e5cc5dc4b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-069-47)  / 470 mL in 1 BOTTLE", "package_ndc": "31722-069-47", "marketing_start_date": "20240117"}], "brand_name": "GABAPENTIN", "product_id": "31722-069_45c076af-c121-6962-e063-6394a90aaad1", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-069", "generic_name": "GABAPENTIN", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA217682", "marketing_category": "ANDA", "marketing_start_date": "20240117", "listing_expiration_date": "20261231"}