Package 17714-133-50

Brand: acetaminophen pm

Generic: acetaminophen pm
NDC Package

Package Facts

Identity

Package NDC 17714-133-50
Digits Only 1771413350
Product NDC 17714-133
Product ID 17714-133_60f41580-e074-faad-e053-2a91aa0a9076
Description

50 TABLET in 1 BOTTLE (17714-133-50)

Marketing

Marketing Status
Marketed Since 2002-01-09
Brand acetaminophen pm
Generic acetaminophen pm
Sample Package No

Linked Drug Pages (1)

ACETAMINOPHEN PM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e074-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714133504"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["b172226e-8f2a-4d9c-b7c7-dd737b90463a"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (17714-133-50)", "package_ndc": "17714-133-50", "marketing_start_date": "20020109"}], "brand_name": "ACETAMINOPHEN PM", "product_id": "17714-133_60f41580-e074-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "17714-133", "generic_name": "ACETAMINOPHEN PM", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20020109", "listing_expiration_date": "20261231"}