ibuprofen 200 mg

Generic: ibuprofen

Labeler: allegiant health
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen 200 mg
Generic Name ibuprofen
Labeler allegiant health
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Allegiant Health

Identifiers & Regulatory

Product NDC 69168-368
Product ID 69168-368_2384fd3b-de52-46c9-bea9-4d8a0342fe59
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079205
Listing Expiration 2026-12-31
Marketing Start 2014-12-22

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 69168368
Hyphenated Format 69168-368

Supplemental Identifiers

RxCUI
310964
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 200 mg (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA079205 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (69168-368-07) / 10 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69168-368-30) / 30 CAPSULE, LIQUID FILLED 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": "2384fd3b-de52-46c9-bea9-4d8a0342fe59", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["8ba06ba0-bfe9-4626-af65-dae4d6a3a2ad"], "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": ["Allegiant Health"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69168-368-07)  / 10 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "69168-368-07", "marketing_start_date": "20141222"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69168-368-30)  / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "69168-368-30", "marketing_start_date": "20141222"}], "brand_name": "Ibuprofen 200 mg", "product_id": "69168-368_2384fd3b-de52-46c9-bea9-4d8a0342fe59", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69168-368", "generic_name": "Ibuprofen", "labeler_name": "Allegiant Health", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen 200 mg", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079205", "marketing_category": "ANDA", "marketing_start_date": "20141222", "listing_expiration_date": "20261231"}