Package 71209-032-04

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 71209-032-04
Digits Only 7120903204
Product NDC 71209-032
Product ID 71209-032_be6557c8-0d68-4313-a689-c2fdfb1d505e
Description

90 CAPSULE in 1 BOTTLE (71209-032-04)

Marketing

Marketing Status
Marketed Since 2023-07-13
Brand pregabalin
Generic pregabalin
Sample Package No

Linked Drug Pages (1)

PREGABALIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "be6557c8-0d68-4313-a689-c2fdfb1d505e", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["170c0c95-2ee8-4dff-bbd6-b87a21e8cf81"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71209-032-04)", "package_ndc": "71209-032-04", "marketing_start_date": "20230713"}], "brand_name": "PREGABALIN", "product_id": "71209-032_be6557c8-0d68-4313-a689-c2fdfb1d505e", "dosage_form": "CAPSULE", "product_ndc": "71209-032", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "25 mg/1"}], "application_number": "ANDA206452", "marketing_category": "ANDA", "marketing_start_date": "20230713", "listing_expiration_date": "20261231"}