Package 49035-181-21

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49035-181-21
Digits Only 4903518121
Product NDC 49035-181
Product ID 49035-181_464fd9d1-4a10-0fb1-e063-6394a90a933d
Description

225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49035-181-21)

Marketing

Marketing Status
Marketed Since 2019-10-04
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "464fd9d1-4a10-0fb1-e063-6394a90a933d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["940936ac-e59f-7489-e053-2a95a90a6364"], "manufacturer_name": ["WAL-MART STORES INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49035-181-21)", "package_ndc": "49035-181-21", "marketing_start_date": "20191004"}], "brand_name": "Acetaminophen", "product_id": "49035-181_464fd9d1-4a10-0fb1-e063-6394a90a933d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "49035-181", "generic_name": "Acetaminophen", "labeler_name": "WAL-MART STORES INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20191004", "listing_expiration_date": "20261231"}