acetaminophen and ibuprofen
Generic: acetaminophen and ibuprofen
Labeler: cvsDrug Facts
Product Profile
Brand Name
acetaminophen and ibuprofen
Generic Name
acetaminophen and ibuprofen
Labeler
cvs
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 250 mg/1, ibuprofen 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51316-131
Product ID
51316-131_46545016-29d2-7e81-e063-6294a90a941f
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA216592
Listing Expiration
2026-12-31
Marketing Start
2023-10-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316131
Hyphenated Format
51316-131
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
acetaminophen and ibuprofen (source: ndc)
Generic Name
acetaminophen and ibuprofen (source: ndc)
Application Number
ANDA216592 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
- 125 mg/1
Packaging
- 36 TABLET in 1 BOTTLE (51316-131-36)
- 144 TABLET in 1 BOTTLE (51316-131-44)
- 72 TABLET in 1 BOTTLE (51316-131-72)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46545016-29d2-7e81-e063-6294a90a941f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["e45830a0-c884-e556-e053-2995a90ab565"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET in 1 BOTTLE (51316-131-36)", "package_ndc": "51316-131-36", "marketing_start_date": "20231001"}, {"sample": false, "description": "144 TABLET in 1 BOTTLE (51316-131-44)", "package_ndc": "51316-131-44", "marketing_start_date": "20231001"}, {"sample": false, "description": "72 TABLET in 1 BOTTLE (51316-131-72)", "package_ndc": "51316-131-72", "marketing_start_date": "20231001"}], "brand_name": "Acetaminophen and Ibuprofen", "product_id": "51316-131_46545016-29d2-7e81-e063-6294a90a941f", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51316-131", "generic_name": "Acetaminophen and Ibuprofen", "labeler_name": "CVS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen and Ibuprofen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216592", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}