Package 71335-2741-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 71335-2741-1
Digits Only 7133527411
Product NDC 71335-2741
Product ID 71335-2741_cd9f3596-223b-483c-9951-2beee373bde2
Description

90 CAPSULE in 1 BOTTLE (71335-2741-1)

Marketing

Marketing Status
Marketed Since 2025-07-28
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": "cd9f3596-223b-483c-9951-2beee373bde2", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["ca8177ed-1f0d-436e-a5ac-f58b8f7cbb25"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-2741-1)", "package_ndc": "71335-2741-1", "marketing_start_date": "20250728"}], "brand_name": "Gabapentin", "product_id": "71335-2741_cd9f3596-223b-483c-9951-2beee373bde2", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2741", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA206943", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}