Package 72162-2262-1
Brand: prochlorperazine maleate
Generic: prochlorperazine maleatePackage Facts
Identity
Package NDC
72162-2262-1
Digits Only
7216222621
Product NDC
72162-2262
Description
100 TABLET in 1 BOTTLE (72162-2262-1)
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": "81434c0c-30a6-4ffd-8f43-1bb84d48ffcc", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["7e3aa80a-3a5f-4937-b5aa-4ce2aa6ece1b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2262-1)", "package_ndc": "72162-2262-1", "marketing_start_date": "20240223"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "72162-2262_81434c0c-30a6-4ffd-8f43-1bb84d48ffcc", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72162-2262", "generic_name": "Prochlorperazine maleate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "19980301", "listing_expiration_date": "20261231"}