Package 43063-447-04

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-447-04
Digits Only 4306344704
Product NDC 43063-447
Product ID 43063-447_2b25624a-3d1a-c6b4-e063-6394a90a4b75
Description

4 TABLET in 1 BOTTLE, PLASTIC (43063-447-04)

Marketing

Marketing Status
Marketed Since 2012-02-21
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": "2b25624a-3d1a-c6b4-e063-6394a90a4b75", "openfda": {"upc": ["0343063447048"], "unii": ["R61ZEH7I1I"], "rxcui": ["992475"], "spl_set_id": ["12400c65-f93b-47a5-8167-1fb14337130b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (43063-447-04)", "package_ndc": "43063-447-04", "marketing_start_date": "20120221"}], "brand_name": "Promethazine Hydrochloride", "product_id": "43063-447_2b25624a-3d1a-c6b4-e063-6394a90a4b75", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43063-447", "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": "50 mg/1"}], "application_number": "ANDA091179", "marketing_category": "ANDA", "marketing_start_date": "20110303", "listing_expiration_date": "20261231"}