ibuprofen

Generic: ibuprofen

Labeler: dolgencorp, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler dolgencorp, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Dolgencorp, Inc.

Identifiers & Regulatory

Product NDC 55910-847
Product ID 55910-847_29a1e9b5-d8dd-c566-e063-6394a90a65c1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2020-03-12

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 55910847
Hyphenated Format 55910-847

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, FILM COATED in 1 BOTTLE (55910-847-02)
  • 2 BOTTLE in 1 CARTON (55910-847-10) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29a1e9b5-d8dd-c566-e063-6394a90a65c1", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["5398f5b7-a9a6-4f7e-a06c-e524b9939562"], "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": ["Dolgencorp, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (55910-847-02)", "package_ndc": "55910-847-02", "marketing_start_date": "20200312"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (55910-847-10)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55910-847-10", "marketing_start_date": "20200312"}], "brand_name": "Ibuprofen", "product_id": "55910-847_29a1e9b5-d8dd-c566-e063-6394a90a65c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55910-847", "generic_name": "Ibuprofen", "labeler_name": "Dolgencorp, Inc.", "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": "20200312", "listing_expiration_date": "20261231"}