dual action

Generic: acetaminophen and ibuprofen (nsaid) tablets, 250 mg/ 125 mg

Labeler: dr. reddy's laboratories inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dual action
Generic Name acetaminophen and ibuprofen (nsaid) tablets, 250 mg/ 125 mg
Labeler dr. reddy's laboratories inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 250 mg/1, ibuprofen 125 mg/1

Manufacturer
Dr. Reddy's Laboratories Inc

Identifiers & Regulatory

Product NDC 75907-158
Product ID 75907-158_ac5bcacf-74a8-2803-2157-fa190e092558
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA218247
Listing Expiration 2026-12-31
Marketing Start 2025-02-06

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75907158
Hyphenated Format 75907-158

Supplemental Identifiers

RxCUI
2387532
UNII
362O9ITL9D WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 dual action (source: ndc)
Generic Name acetaminophen and ibuprofen (nsaid) tablets, 250 mg/ 125 mg (source: ndc)
Application Number ANDA218247 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 144 TABLET, FILM COATED in 1 BOTTLE (75907-158-14)
  • 250 TABLET, FILM COATED in 1 BOTTLE (75907-158-25)
source: ndc

Packages (2)

75907-158-14 144 TABLET, FILM COATED in 1 BOTTLE (75907-158-14) 75907-158-25 250 TABLET, FILM COATED in 1 BOTTLE (75907-158-25)

Ingredients (2)

acetaminophen (250 mg/1) ibuprofen (125 mg/1)

Linked Drug Pages (1)

Dual Action ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ac5bcacf-74a8-2803-2157-fa190e092558", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["c8a8a18a-6766-37a9-d0f0-f9380fb5b0e8"], "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 Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "144 TABLET, FILM COATED in 1 BOTTLE (75907-158-14)", "package_ndc": "75907-158-14", "marketing_start_date": "20250206"}, {"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE (75907-158-25)", "package_ndc": "75907-158-25", "marketing_start_date": "20250206"}], "brand_name": "Dual Action", "product_id": "75907-158_ac5bcacf-74a8-2803-2157-fa190e092558", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "75907-158", "generic_name": "Acetaminophen and Ibuprofen (NSAID) Tablets, 250 mg/ 125 mg", "labeler_name": "Dr. Reddy's Laboratories Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dual Action", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA218247", "marketing_category": "ANDA", "marketing_start_date": "20250206", "listing_expiration_date": "20261231"}