ibuprofen

Generic: ibuprofen

Labeler: geri-care pharmaceutical corp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler geri-care pharmaceutical corp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Geri-Care Pharmaceutical Corp

Identifiers & Regulatory

Product NDC 57896-941
Product ID 57896-941_08f1bde2-f476-2d2f-e063-6294a90a6f93
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075010
Listing Expiration 2026-12-31
Marketing Start 2004-01-01

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 57896941
Hyphenated Format 57896-941

Supplemental Identifiers

RxCUI
310965
UPC
0357896941017
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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA075010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (57896-941-01)
  • 50 TABLET, FILM COATED in 1 BOTTLE (57896-941-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (57896-941-10)
  • 1 BOTTLE in 1 CARTON (57896-941-20) / 200 TABLET, FILM COATED in 1 BOTTLE
  • 500 TABLET, FILM COATED in 1 BOTTLE (57896-941-50)
source: ndc

Packages (5)

57896-941-01 100 TABLET, FILM COATED in 1 BOTTLE (57896-941-01) 57896-941-05 50 TABLET, FILM COATED in 1 BOTTLE (57896-941-05) 57896-941-10 1000 TABLET, FILM COATED in 1 BOTTLE (57896-941-10) 57896-941-20 1 BOTTLE in 1 CARTON (57896-941-20) / 200 TABLET, FILM COATED in 1 BOTTLE 57896-941-50 500 TABLET, FILM COATED in 1 BOTTLE (57896-941-50)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08f1bde2-f476-2d2f-e063-6294a90a6f93", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0357896941017"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["0744c3ca-4224-4f6a-a033-880949b544fd"], "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": ["Geri-Care Pharmaceutical Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (57896-941-01)", "package_ndc": "57896-941-01", "marketing_start_date": "20170901"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (57896-941-05)", "package_ndc": "57896-941-05", "marketing_start_date": "20170901"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (57896-941-10)", "package_ndc": "57896-941-10", "marketing_start_date": "20170901"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (57896-941-20)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "57896-941-20", "marketing_start_date": "20120201"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (57896-941-50)", "package_ndc": "57896-941-50", "marketing_start_date": "20170901"}], "brand_name": "Ibuprofen", "product_id": "57896-941_08f1bde2-f476-2d2f-e063-6294a90a6f93", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "57896-941", "generic_name": "ibuprofen", "labeler_name": "Geri-Care Pharmaceutical Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "20040101", "listing_expiration_date": "20261231"}