motrin ib

Generic: ibuprofen

Labeler: morning star otc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name motrin ib
Generic Name ibuprofen
Labeler morning star otc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Morning Star OTC

Identifiers & Regulatory

Product NDC 53209-2001
Product ID 53209-2001_37e92a7b-971f-c212-e063-6394a90ad710
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077349
Listing Expiration 2026-12-31
Marketing Start 2025-06-19

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 532092001
Hyphenated Format 53209-2001

Supplemental Identifiers

RxCUI
201126 310965
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 motrin ib (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA077349 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 25 BLISTER PACK in 1 POUCH (53209-2001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-2001-1)
source: ndc

Packages (1)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37e92a7b-971f-c212-e063-6394a90ad710", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["201126", "310965"], "spl_set_id": ["e69f00c4-b8ec-4a83-9eea-8cb2835ad776"], "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": ["Morning Star OTC"]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 POUCH (53209-2001-2)  / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-2001-1)", "package_ndc": "53209-2001-2", "marketing_start_date": "20250619"}], "brand_name": "Motrin IB", "product_id": "53209-2001_37e92a7b-971f-c212-e063-6394a90ad710", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53209-2001", "generic_name": "Ibuprofen", "labeler_name": "Morning Star OTC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motrin IB", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA077349", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}