Package 0904-6992-61

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 0904-6992-61
Digits Only 0904699261
Product NDC 0904-6992
Description

100 BLISTER PACK in 1 CARTON (0904-6992-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-07-19
Brand pregabalin
Generic pregabalin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ce6f3554-3f28-4d2e-8f32-e0893f1f43a5", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["2420e2d7-c01a-4590-88c5-6fe5361747e9"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6992-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6992-61", "marketing_start_date": "20190719"}], "brand_name": "PREGABALIN", "product_id": "0904-6992_ce6f3554-3f28-4d2e-8f32-e0893f1f43a5", "dosage_form": "CAPSULE", "product_ndc": "0904-6992", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "50 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}