good sense ibuprofen

Generic: ibuprofen

Labeler: l. perrigo company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name good sense ibuprofen
Generic Name ibuprofen
Labeler l. perrigo company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
L. Perrigo Company

Identifiers & Regulatory

Product NDC 0113-0604
Product ID 0113-0604_822f5bcb-7dcf-454a-8d76-8ce8aaa40d4c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA072096
Listing Expiration 2026-12-31
Marketing Start 1989-09-15

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 01130604
Hyphenated Format 0113-0604

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 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
  • 1 BOTTLE in 1 CARTON (0113-0604-62) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0113-0604-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0113-0604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (0113-0604-82) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 500 TABLET, FILM COATED in 1 BOTTLE (0113-0604-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (0113-0604-93)
source: ndc

Packages (6)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "822f5bcb-7dcf-454a-8d76-8ce8aaa40d4c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["70d0a429-27c1-43a5-b2ea-a9919e0910f8"], "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": ["L. Perrigo Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0604-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0604-62", "marketing_start_date": "19920504"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0604-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0604-71", "marketing_start_date": "19890915"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0604-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0604-78", "marketing_start_date": "19890915"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (0113-0604-82)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0604-82", "marketing_start_date": "20110302"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0113-0604-90)", "package_ndc": "0113-0604-90", "marketing_start_date": "19930118"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0113-0604-93)", "package_ndc": "0113-0604-93", "marketing_start_date": "20070531"}], "brand_name": "good sense ibuprofen", "product_id": "0113-0604_822f5bcb-7dcf-454a-8d76-8ce8aaa40d4c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0113-0604", "generic_name": "Ibuprofen", "labeler_name": "L. Perrigo Company", "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": "19890915", "listing_expiration_date": "20261231"}