ibuprofen

Generic: ibuprofen

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler rite aid corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
RITE AID CORPORATION

Identifiers & Regulatory

Product NDC 11822-7892
Product ID 11822-7892_cf2caf6f-2192-2428-e053-2995a90aae6d
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091239
Listing Expiration 2026-12-31
Marketing Start 2020-06-01

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 118227892
Hyphenated Format 11822-7892

Supplemental Identifiers

RxCUI
310965
UPC
0011822789158 0011822789141 0011822789134 0011822789127 0011822789165
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 ANDA091239 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 24 TABLET, COATED in 1 BOTTLE (11822-7892-0)
  • 50 TABLET, COATED in 1 BOTTLE (11822-7892-2)
  • 100 TABLET, COATED in 1 BOTTLE (11822-7892-5)
  • 200 TABLET, COATED in 1 BOTTLE (11822-7892-7)
  • 500 TABLET, COATED in 1 BOTTLE (11822-7892-9)
source: ndc

Packages (5)

11822-7892-0 24 TABLET, COATED in 1 BOTTLE (11822-7892-0) 11822-7892-2 50 TABLET, COATED in 1 BOTTLE (11822-7892-2) 11822-7892-5 100 TABLET, COATED in 1 BOTTLE (11822-7892-5) 11822-7892-7 200 TABLET, COATED in 1 BOTTLE (11822-7892-7) 11822-7892-9 500 TABLET, COATED in 1 BOTTLE (11822-7892-9)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

IBUPROFEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf2caf6f-2192-2428-e053-2995a90aae6d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0011822789158", "0011822789141", "0011822789134", "0011822789127", "0011822789165"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["a7abac4c-7695-cfe8-e053-2a95a90ac1cd"], "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": ["RITE AID CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, COATED in 1 BOTTLE (11822-7892-0)", "package_ndc": "11822-7892-0", "marketing_start_date": "20200601"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (11822-7892-2)", "package_ndc": "11822-7892-2", "marketing_start_date": "20200601"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (11822-7892-5)", "package_ndc": "11822-7892-5", "marketing_start_date": "20200601"}, {"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (11822-7892-7)", "package_ndc": "11822-7892-7", "marketing_start_date": "20200601"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (11822-7892-9)", "package_ndc": "11822-7892-9", "marketing_start_date": "20200601"}], "brand_name": "IBUPROFEN", "product_id": "11822-7892_cf2caf6f-2192-2428-e053-2995a90aae6d", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11822-7892", "generic_name": "IBUPROFEN", "labeler_name": "RITE AID CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}