ibuprofen

Generic: ibuprofen 200mg

Labeler: advanced first aid, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen 200mg
Labeler advanced first aid, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
ADVANCED FIRST AID, INC.

Identifiers & Regulatory

Product NDC 67060-001
Product ID 67060-001_feb250d0-cddb-448d-b08d-00a0fc091055
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2015-04-09

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 67060001
Hyphenated Format 67060-001

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 200mg (source: ndc)
Application Number ANDA079174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 250 PACKET in 1 CARTON (67060-001-67) / 2 TABLET, FILM COATED in 1 PACKET
  • 100 PACKET in 1 CARTON (67060-001-68) / 2 TABLET, FILM COATED in 1 PACKET
source: ndc

Packages (2)

67060-001-67 250 PACKET in 1 CARTON (67060-001-67) / 2 TABLET, FILM COATED in 1 PACKET 67060-001-68 100 PACKET in 1 CARTON (67060-001-68) / 2 TABLET, FILM COATED in 1 PACKET

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": "feb250d0-cddb-448d-b08d-00a0fc091055", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["564e9910-b491-4129-a4f1-68216267623b"], "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": ["ADVANCED FIRST AID, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 PACKET in 1 CARTON (67060-001-67)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "67060-001-67", "marketing_start_date": "20150409"}, {"sample": false, "description": "100 PACKET in 1 CARTON (67060-001-68)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "67060-001-68", "marketing_start_date": "20150409"}], "brand_name": "IBUPROFEN", "product_id": "67060-001_feb250d0-cddb-448d-b08d-00a0fc091055", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67060-001", "generic_name": "IBUPROFEN 200MG", "labeler_name": "ADVANCED FIRST AID, 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": "20150409", "listing_expiration_date": "20261231"}