Package 0904-7381-06
Brand: prochlorperazine maleate
Generic: prochlorperazine maleatePackage Facts
Identity
Package NDC
0904-7381-06
Digits Only
0904738106
Product NDC
0904-7381
Description
50 BLISTER PACK in 1 CARTON (0904-7381-06) / 1 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
prochlorperazine maleate
Generic
prochlorperazine maleate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8293831f-a230-4ae6-8e93-be496e20b7e7", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["d6fc83ad-9cce-4e60-854c-3825313ee60c"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7381-06) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7381-06", "marketing_start_date": "20231030"}], "brand_name": "Prochlorperazine Maleate", "product_id": "0904-7381_8293831f-a230-4ae6-8e93-be496e20b7e7", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-7381", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA216202", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}