ibu

Generic: ibu

Labeler: redpharm drug, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibu
Generic Name ibu
Labeler redpharm drug, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-0913
Product ID 67296-0913_3251a7a8-7561-cf22-e063-6394a90adcb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075682
Listing Expiration 2026-12-31
Marketing Start 2008-11-20

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 672960913
Hyphenated Format 67296-0913

Supplemental Identifiers

RxCUI
197806
UPC
0367296091311
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 ibu (source: ndc)
Generic Name ibu (source: ndc)
Application Number ANDA075682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (67296-0913-1)
  • 10 TABLET in 1 BOTTLE (67296-0913-3)
  • 90 TABLET in 1 BOTTLE (67296-0913-9)
source: ndc

Packages (3)

67296-0913-1 30 TABLET in 1 BOTTLE (67296-0913-1) 67296-0913-3 10 TABLET in 1 BOTTLE (67296-0913-3) 67296-0913-9 90 TABLET in 1 BOTTLE (67296-0913-9)

Ingredients (1)

ibuprofen (600 mg/1)

Linked Drug Pages (1)

IBU ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3251a7a8-7561-cf22-e063-6394a90adcb3", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0367296091311"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["4db219dc-ea48-490c-e054-00144ff88e88"], "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": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-0913-1)", "package_ndc": "67296-0913-1", "marketing_start_date": "20081120"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (67296-0913-3)", "package_ndc": "67296-0913-3", "marketing_start_date": "20081120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (67296-0913-9)", "package_ndc": "67296-0913-9", "marketing_start_date": "20081120"}], "brand_name": "IBU", "product_id": "67296-0913_3251a7a8-7561-cf22-e063-6394a90adcb3", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67296-0913", "generic_name": "IBU", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBU", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20081120", "listing_expiration_date": "20261231"}