uline ibuprofen

Generic: ibuprofen

Labeler: uline
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name uline ibuprofen
Generic Name ibuprofen
Labeler uline
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Uline

Identifiers & Regulatory

Product NDC 69790-609
Product ID 69790-609_3e5d77e9-9142-41d7-e063-6294a90a365e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075010
Listing Expiration 2026-12-31
Marketing Start 2022-04-04

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 69790609
Hyphenated Format 69790-609

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 uline ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA075010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 50 PACKET in 1 BOX (69790-609-33) / 2 TABLET, COATED in 1 PACKET
source: ndc

Packages (1)

69790-609-33 50 PACKET in 1 BOX (69790-609-33) / 2 TABLET, COATED in 1 PACKET

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Uline Ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e5d77e9-9142-41d7-e063-6294a90a365e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["d7342a15-9d49-74ed-e053-2a95a90a22cc"], "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": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (69790-609-33)  / 2 TABLET, COATED in 1 PACKET", "package_ndc": "69790-609-33", "marketing_start_date": "20220404"}], "brand_name": "Uline Ibuprofen", "product_id": "69790-609_3e5d77e9-9142-41d7-e063-6294a90a365e", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69790-609", "generic_name": "Ibuprofen", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uline Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "20220404", "listing_expiration_date": "20261231"}