Package 60687-660-01

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-660-01
Digits Only 6068766001
Product NDC 60687-660
Product ID 60687-660_437eb3f4-c605-1e34-e063-6294a90aba73
Description

100 BLISTER PACK in 1 CARTON (60687-660-01) / 1 TABLET in 1 BLISTER PACK (60687-660-11)

Marketing

Marketing Status
Marketed Since 2022-06-20
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": "437eb3f4-c605-1e34-e063-6294a90aba73", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992438"], "spl_set_id": ["57b4bf23-c563-4357-9dcf-066cbc1280e4"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-660-01)  / 1 TABLET in 1 BLISTER PACK (60687-660-11)", "package_ndc": "60687-660-01", "marketing_start_date": "20220620"}], "brand_name": "Promethazine Hydrochloride", "product_id": "60687-660_437eb3f4-c605-1e34-e063-6294a90aba73", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60687-660", "generic_name": "Promethazine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20220620", "listing_expiration_date": "20261231"}