ibuprofen 200 mg (0761-0908)

Drug Facts

Product Profile

Brand Name ibuprofen 200 mg

Generic Name ibuprofen

Labeler basic drugs, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

ibuprofen 200 mg/1

Manufacturer

Basic Drugs, Inc.

Identifiers & Regulatory

Product NDC 0761-0908

Product ID 0761-0908_0e12b3c6-3579-b0dc-e063-6394a90a8ea4

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA079174

Listing Expiration 2026-12-31

Marketing Start 2021-12-14

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 07610908

Hyphenated Format 0761-0908

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 200 mg (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

250 TABLET in 1 BOTTLE (0761-0908-04)

source: ndc

Packages (1)

0761-0908-04 250 TABLET in 1 BOTTLE (0761-0908-04)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

IBUPROFEN 200 MG ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "0e12b3c6-3579-b0dc-e063-6394a90a8ea4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["d3351d44-2078-3adc-e053-2995a90a3c8f"], "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": ["Basic Drugs, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET in 1 BOTTLE (0761-0908-04)", "package_ndc": "0761-0908-04", "marketing_start_date": "20211215"}], "brand_name": "IBUPROFEN 200 MG", "product_id": "0761-0908_0e12b3c6-3579-b0dc-e063-6394a90a8ea4", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0761-0908", "generic_name": "IBUPROFEN", "labeler_name": "Basic Drugs, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "brand_name_suffix": "200 MG", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}