Package 43063-875-01

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-875-01
Digits Only 4306387501
Product NDC 43063-875
Product ID 43063-875_415c4f6b-6dfe-2bc2-e063-6394a90ae1af
Description

100 TABLET in 1 BOTTLE, PLASTIC (43063-875-01)

Marketing

Marketing Status
Marketed Since 2018-08-17
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

PROMETHAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "415c4f6b-6dfe-2bc2-e063-6394a90ae1af", "openfda": {"upc": ["0343063875018"], "unii": ["R61ZEH7I1I"], "rxcui": ["992438"], "spl_set_id": ["b0ba50da-9f70-4531-a9de-3dd3f8aa1f5d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-875-01)", "package_ndc": "43063-875-01", "marketing_start_date": "20180817"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "43063-875_415c4f6b-6dfe-2bc2-e063-6394a90ae1af", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43063-875", "generic_name": "promethazine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20261231"}