Package 0591-5319-01

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-5319-01
Digits Only 0591531901
Product NDC 0591-5319
Product ID 0591-5319_4ad005c9-31b6-4232-995f-920d1839256e
Description

100 TABLET in 1 BOTTLE, PLASTIC (0591-5319-01)

Marketing

Marketing Status
Marketed Since 1973-09-21
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": "4ad005c9-31b6-4232-995f-920d1839256e", "openfda": {"upc": ["0305915319019", "0305915307016"], "unii": ["R61ZEH7I1I"], "rxcui": ["992447", "992475"], "spl_set_id": ["a32255f0-0077-489e-bdc6-869aca8cd434"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-5319-01)", "package_ndc": "0591-5319-01", "marketing_start_date": "19730921"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0591-5319_4ad005c9-31b6-4232-995f-920d1839256e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0591-5319", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA083711", "marketing_category": "ANDA", "marketing_start_date": "19730921", "listing_expiration_date": "20261231"}