unishield ibuprofen

Generic: ibuprofen

Labeler: unishield
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name unishield ibuprofen
Generic Name ibuprofen
Labeler unishield
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Unishield

Identifiers & Regulatory

Product NDC 49314-1003
Product ID 49314-1003_3e5d6ccc-f765-21b5-e063-6394a90a3400
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

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 493141003
Hyphenated Format 49314-1003

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 unishield 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
  • 50 PACKET in 1 BOX (49314-1003-3) / 2 TABLET, COATED in 1 PACKET
source: ndc

Packages (1)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e5d6ccc-f765-21b5-e063-6394a90a3400", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["b9e2e2ba-e2ad-eace-e053-2995a90aed35"], "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": ["Unishield"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (49314-1003-3)  / 2 TABLET, COATED in 1 PACKET", "package_ndc": "49314-1003-3", "marketing_start_date": "20210301"}], "brand_name": "Unishield Ibuprofen", "product_id": "49314-1003_3e5d6ccc-f765-21b5-e063-6394a90a3400", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49314-1003", "generic_name": "Ibuprofen", "labeler_name": "Unishield", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Unishield Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}