Package 51655-085-20

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-085-20
Digits Only 5165508520
Product NDC 51655-085
Description

20 TABLET in 1 BOTTLE, PLASTIC (51655-085-20)

Marketing

Marketing Status
Marketed Since 2022-10-14
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": "46ddd736-abb2-356b-e063-6394a90a9e76", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["ba4ec2d8-1da4-473b-9ef8-57051cb2c0f7"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-085-20)", "package_ndc": "51655-085-20", "marketing_start_date": "20221014"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, DISPENSING (51655-085-53)", "package_ndc": "51655-085-53", "marketing_start_date": "20140601"}], "brand_name": "Promethazine Hydrochloride", "product_id": "51655-085_46ddd736-abb2-356b-e063-6394a90a9e76", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51655-085", "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": "ANDA091179", "marketing_category": "ANDA", "marketing_start_date": "20140601", "listing_expiration_date": "20271231"}