acetaminophen 250 mg and ibuprofen 125 mg
Generic: acetaminophen and ibuprofen
Labeler: dr. reddy's labortories incDrug Facts
Product Profile
Brand Name
acetaminophen 250 mg and ibuprofen 125 mg
Generic Name
acetaminophen and ibuprofen
Labeler
dr. reddy's labortories inc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 250 mg/1, ibuprofen 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-052
Product ID
43598-052_49a54544-f18b-6461-9ed0-2740e8df4b6c
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA218247
Listing Expiration
2026-12-31
Marketing Start
2025-02-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598052
Hyphenated Format
43598-052
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 250 mg and ibuprofen 125 mg (source: ndc)
Generic Name
acetaminophen and ibuprofen (source: ndc)
Application Number
ANDA218247 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
- 125 mg/1
Packaging
- 500 TABLET, FILM COATED in 1 BOTTLE (43598-052-05)
- 144 TABLET, FILM COATED in 1 BOTTLE (43598-052-14)
- 1 BOTTLE in 1 CARTON (43598-052-18) / 18 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (43598-052-25) / 250 TABLET, FILM COATED in 1 BOTTLE
- 250 TABLET, FILM COATED in 1 BOTTLE (43598-052-95)
Packages (5)
43598-052-05
500 TABLET, FILM COATED in 1 BOTTLE (43598-052-05)
43598-052-14
144 TABLET, FILM COATED in 1 BOTTLE (43598-052-14)
43598-052-18
1 BOTTLE in 1 CARTON (43598-052-18) / 18 TABLET, FILM COATED in 1 BOTTLE
43598-052-25
1 BOTTLE in 1 CARTON (43598-052-25) / 250 TABLET, FILM COATED in 1 BOTTLE
43598-052-95
250 TABLET, FILM COATED in 1 BOTTLE (43598-052-95)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49a54544-f18b-6461-9ed0-2740e8df4b6c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["3e65c8a3-498e-1a2a-bb76-18e28ae2c73c"], "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": ["Dr. Reddy's Labortories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43598-052-05)", "package_ndc": "43598-052-05", "marketing_start_date": "20250219"}, {"sample": false, "description": "144 TABLET, FILM COATED in 1 BOTTLE (43598-052-14)", "package_ndc": "43598-052-14", "marketing_start_date": "20250219"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-052-18) / 18 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "43598-052-18", "marketing_start_date": "20250219"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-052-25) / 250 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "43598-052-25", "marketing_start_date": "20250219"}, {"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE (43598-052-95)", "package_ndc": "43598-052-95", "marketing_start_date": "20250219"}], "brand_name": "Acetaminophen 250 mg and Ibuprofen 125 mg", "product_id": "43598-052_49a54544-f18b-6461-9ed0-2740e8df4b6c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43598-052", "generic_name": "Acetaminophen and Ibuprofen", "labeler_name": "Dr. Reddy's Labortories Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen 250 mg and Ibuprofen 125 mg", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA218247", "marketing_category": "ANDA", "marketing_start_date": "20250219", "listing_expiration_date": "20261231"}