ibuprofen

Generic: ibuprofen

Labeler: bi-mart
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler bi-mart
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Bi-Mart

Identifiers & Regulatory

Product NDC 37835-581
Product ID 37835-581_2eb89807-b8b2-e482-e063-6294a90aea80
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2011-01-01

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 37835581
Hyphenated Format 37835-581

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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA079174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (37835-581-01)
  • 500 TABLET in 1 BOTTLE (37835-581-05)
  • 1000 TABLET in 1 BOTTLE (37835-581-10)
  • 250 TABLET in 1 BOTTLE (37835-581-25)
source: ndc

Packages (4)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2eb89807-b8b2-e482-e063-6294a90aea80", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["7ceacd63-d5fa-4cab-b8f3-a5131c97bb90"], "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": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37835-581-01)", "package_ndc": "37835-581-01", "marketing_start_date": "20250201"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (37835-581-05)", "package_ndc": "37835-581-05", "marketing_start_date": "20250201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (37835-581-10)", "package_ndc": "37835-581-10", "marketing_start_date": "20250201"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (37835-581-25)", "package_ndc": "37835-581-25", "marketing_start_date": "20250201"}], "brand_name": "Ibuprofen", "product_id": "37835-581_2eb89807-b8b2-e482-e063-6294a90aea80", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37835-581", "generic_name": "Ibuprofen", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20110101", "listing_expiration_date": "20261231"}