Package 42708-103-12

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-103-12
Digits Only 4270810312
Product NDC 42708-103
Product ID 42708-103_4682c28f-fee2-11c4-e063-6294a90a2342
Description

12 TABLET in 1 BOTTLE (42708-103-12)

Marketing

Marketing Status
Marketed Since 2019-10-18
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package Yes

Linked Drug Pages (1)

PROCHLORPERAZINE MALEATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4682c28f-fee2-11c4-e063-6294a90a2342", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["dc692e77-5240-4aa6-8fe9-9ffcbb267261"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "12 TABLET in 1 BOTTLE (42708-103-12)", "package_ndc": "42708-103-12", "marketing_start_date": "20191018"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "42708-103_4682c28f-fee2-11c4-e063-6294a90a2342", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "42708-103", "generic_name": "Prochlorperazine maleate", "labeler_name": "QPharma, Inc.", "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"}