good sense ibuprofen

Generic: ibuprofen

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name good sense ibuprofen
Generic Name ibuprofen
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-4051
Product ID 68788-4051_c447fc6b-e9ef-447a-9609-5f893e18dfa7
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA072096
Listing Expiration 2026-12-31
Marketing Start 2025-11-17

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 687884051
Hyphenated Format 68788-4051

Supplemental Identifiers

RxCUI
310965
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 good sense ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA072096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-4051-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-4051-3)
  • 50 TABLET, FILM COATED in 1 BOTTLE (68788-4051-5)
source: ndc

Packages (3)

68788-4051-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-4051-1) 68788-4051-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-4051-3) 68788-4051-5 50 TABLET, FILM COATED in 1 BOTTLE (68788-4051-5)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

good sense ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c447fc6b-e9ef-447a-9609-5f893e18dfa7", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["c447fc6b-e9ef-447a-9609-5f893e18dfa7"], "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": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-4051-1)", "package_ndc": "68788-4051-1", "marketing_start_date": "20251117"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-4051-3)", "package_ndc": "68788-4051-3", "marketing_start_date": "20251117"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (68788-4051-5)", "package_ndc": "68788-4051-5", "marketing_start_date": "20251117"}], "brand_name": "good sense ibuprofen", "product_id": "68788-4051_c447fc6b-e9ef-447a-9609-5f893e18dfa7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-4051", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "good sense ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "20251117", "listing_expiration_date": "20261231"}