cabinet pain reliever and fever reducer

Generic: ibuprofen

Labeler: spirit pharmaceutical llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cabinet pain reliever and fever reducer
Generic Name ibuprofen
Labeler spirit pharmaceutical llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Spirit Pharmaceutical LLC

Identifiers & Regulatory

Product NDC 68210-0026
Product ID 68210-0026_2a8259ca-1448-91b8-e063-6394a90a7057
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2019-10-30

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 682100026
Hyphenated Format 68210-0026

Supplemental Identifiers

RxCUI
310965
UNII
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 cabinet pain reliever and fever reducer (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA079174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0026-1)
  • 1 BOTTLE, PLASTIC in 1 CARTON (68210-0026-2) / 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

68210-0026-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0026-1) 68210-0026-2 1 BOTTLE, PLASTIC in 1 CARTON (68210-0026-2) / 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Cabinet Pain Reliever and Fever Reducer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a8259ca-1448-91b8-e063-6394a90a7057", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["e172a8d8-779d-4ad9-b6b0-08a198a58034"], "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": ["Spirit Pharmaceutical LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0026-1)", "package_ndc": "68210-0026-1", "marketing_start_date": "20191030"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68210-0026-2)  / 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68210-0026-2", "marketing_start_date": "20191030"}], "brand_name": "Cabinet Pain Reliever and Fever Reducer", "product_id": "68210-0026_2a8259ca-1448-91b8-e063-6394a90a7057", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68210-0026", "generic_name": "Ibuprofen", "labeler_name": "Spirit Pharmaceutical LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cabinet Pain Reliever and Fever Reducer", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20191030", "listing_expiration_date": "20261231"}