Package 0904-5847-09

Brand: extra strength acetaminohpen adult rapid burst cherry

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0904-5847-09
Digits Only 0904584709
Product NDC 0904-5847
Description

237 mL in 1 BOTTLE, PLASTIC (0904-5847-09)

Marketing

Marketing Status
Discontinued 2026-11-28
Brand extra strength acetaminohpen adult rapid burst cherry
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "528a4d65-08dc-4bec-8587-eb0c096dd8d1", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["9e7543d9-6249-45b5-b67d-c1b439423b9c"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (0904-5847-09)", "package_ndc": "0904-5847-09", "marketing_end_date": "20261128", "marketing_start_date": "20090702"}], "brand_name": "Extra Strength Acetaminohpen Adult Rapid Burst Cherry", "product_id": "0904-5847_528a4d65-08dc-4bec-8587-eb0c096dd8d1", "dosage_form": "LIQUID", "product_ndc": "0904-5847", "generic_name": "Acetaminophen", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminohpen", "brand_name_suffix": "Adult Rapid Burst Cherry", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261128", "marketing_start_date": "20090702"}