ibuprofen

Generic: ibuprofen

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

Drug Facts

Product Profile

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

ibuprofen 200 mg/1

Manufacturer
INGLES MARKETS, INC.

Identifiers & Regulatory

Product NDC 62936-0941
Product ID 62936-0941_efa5fff1-3a7a-202e-e053-2a95a90add3a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075010
Listing Expiration 2026-12-31
Marketing Start 2004-01-01

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 629360941
Hyphenated Format 62936-0941

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 ANDA075010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (62936-0941-1) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (62936-0941-5) / 50 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (2)

62936-0941-1 1 BOTTLE in 1 CARTON (62936-0941-1) / 100 TABLET, FILM COATED in 1 BOTTLE 62936-0941-5 1 BOTTLE in 1 CARTON (62936-0941-5) / 50 TABLET, FILM COATED in 1 BOTTLE

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": "efa5fff1-3a7a-202e-e053-2a95a90add3a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["ef536841-768c-919f-e053-2a95a90af599"], "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": ["INGLES MARKETS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (62936-0941-1)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "62936-0941-1", "marketing_start_date": "20221101"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (62936-0941-5)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "62936-0941-5", "marketing_start_date": "20221101"}], "brand_name": "Ibuprofen", "product_id": "62936-0941_efa5fff1-3a7a-202e-e053-2a95a90add3a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "62936-0941", "generic_name": "ibuprofen", "labeler_name": "INGLES MARKETS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "20040101", "listing_expiration_date": "20261231"}