Package 51655-140-52

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-140-52
Digits Only 5165514052
Product NDC 51655-140
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-140-52)

Marketing

Marketing Status
Marketed Since 2023-02-03
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c3d54f-f13b-5a44-e063-6394a90aa096", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["f6ca1097-1c75-c682-e053-6294a90a2bd6"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-140-52)", "package_ndc": "51655-140-52", "marketing_start_date": "20230203"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (51655-140-53)", "package_ndc": "51655-140-53", "marketing_start_date": "20230203"}], "brand_name": "Promethazine Hydrochloride", "product_id": "51655-140_48c3d54f-f13b-5a44-e063-6394a90aa096", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51655-140", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA083426", "marketing_category": "ANDA", "marketing_start_date": "20230203", "listing_expiration_date": "20271231"}