ibuprofen

Generic: ibuprofen

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-212
Product ID 72789-212_341805b5-3ae2-802f-e063-6294a90a9e17
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078329
Listing Expiration 2026-12-31
Marketing Start 2020-08-21

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 72789212
Hyphenated Format 72789-212

Supplemental Identifiers

RxCUI
197806
UPC
0372789212159
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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA078329 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-06)
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-10)
  • 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-15)
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-20)
  • 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-21)
  • 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-24)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-30)
  • 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-40)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-90)
source: ndc

Packages (9)

72789-212-06 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-06) 72789-212-10 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-10) 72789-212-15 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-15) 72789-212-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-20) 72789-212-21 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-21) 72789-212-24 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-24) 72789-212-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-30) 72789-212-40 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-40) 72789-212-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-90)

Ingredients (1)

ibuprofen (600 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": "341805b5-3ae2-802f-e063-6294a90a9e17", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0372789212159"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["09621787-9a5c-4abf-9ccd-d6f8d581738f"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-06)", "package_ndc": "72789-212-06", "marketing_start_date": "20220802"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-10)", "package_ndc": "72789-212-10", "marketing_start_date": "20220802"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-15)", "package_ndc": "72789-212-15", "marketing_start_date": "20211027"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-20)", "package_ndc": "72789-212-20", "marketing_start_date": "20211119"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-21)", "package_ndc": "72789-212-21", "marketing_start_date": "20200821"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-24)", "package_ndc": "72789-212-24", "marketing_start_date": "20211026"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-30)", "package_ndc": "72789-212-30", "marketing_start_date": "20211019"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-40)", "package_ndc": "72789-212-40", "marketing_start_date": "20220103"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-90)", "package_ndc": "72789-212-90", "marketing_start_date": "20211025"}], "brand_name": "Ibuprofen", "product_id": "72789-212_341805b5-3ae2-802f-e063-6294a90a9e17", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-212", "generic_name": "Ibuprofen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20200821", "listing_expiration_date": "20261231"}