ibuwin forte

Generic: ibuprofen

Labeler: opmx llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuwin forte
Generic Name ibuprofen
Labeler opmx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
OPMX LLC

Identifiers & Regulatory

Product NDC 69729-157
Product ID 69729-157_0daf1b9c-b64c-5616-e063-6294a90ab3c2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2023-12-29

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 69729157
Hyphenated Format 69729-157

Supplemental Identifiers

RxCUI
310965
UPC
0810053181416
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 ibuwin forte (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
  • 1 BLISTER PACK in 1 CARTON (69729-157-10) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

69729-157-10 1 BLISTER PACK in 1 CARTON (69729-157-10) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Ibuwin Forte ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0daf1b9c-b64c-5616-e063-6294a90ab3c2", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0810053181416"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["0daf1be9-ea38-461e-e063-6394a90a7954"], "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": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69729-157-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "69729-157-10", "marketing_start_date": "20231229"}], "brand_name": "Ibuwin Forte", "product_id": "69729-157_0daf1b9c-b64c-5616-e063-6294a90ab3c2", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69729-157", "generic_name": "Ibuprofen", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuwin Forte", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20231229", "listing_expiration_date": "20261231"}