Package 10702-004-10

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-004-10
Digits Only 1070200410
Product NDC 10702-004
Product ID 10702-004_17529733-d03d-6be0-e063-6294a90a99bf
Description

1000 TABLET in 1 BOTTLE (10702-004-10)

Marketing

Marketing Status
Marketed Since 2006-07-31
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": "17529733-d03d-6be0-e063-6294a90a99bf", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992438", "992447", "992475"], "spl_set_id": ["7a137adf-39b7-4b14-80da-c3cac9ad562a"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-004-01)", "package_ndc": "10702-004-01", "marketing_start_date": "20060731"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-004-10)", "package_ndc": "10702-004-10", "marketing_start_date": "20060731"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "10702-004_17529733-d03d-6be0-e063-6294a90a99bf", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "10702-004", "generic_name": "promethazine hydrochloride", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20060731", "listing_expiration_date": "20261231"}