ibuprofen

Generic: ibuprofen tablet, film-coated

Labeler: lil' drug store products, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen tablet, film-coated
Labeler lil' drug store products, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Lil' Drug Store Products, Inc.

Identifiers & Regulatory

Product NDC 66715-9819
Product ID 66715-9819_e5bf5e09-7d43-6314-e053-2a95a90a2325
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075010
Listing Expiration 2026-12-31
Marketing Start 2014-09-12

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 667159819
Hyphenated Format 66715-9819

Supplemental Identifiers

RxCUI
310965
UPC
0366715971975
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 tablet, film-coated (source: ndc)
Application Number ANDA075010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 50 POUCH in 1 BOX, UNIT-DOSE (66715-9819-7) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

66715-9819-7 50 POUCH in 1 BOX, UNIT-DOSE (66715-9819-7) / 2 TABLET, FILM COATED in 1 POUCH

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": "e5bf5e09-7d43-6314-e053-2a95a90a2325", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0366715971975"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["e5bf5e09-7d42-6314-e053-2a95a90a2325"], "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": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (66715-9819-7)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-9819-7", "marketing_start_date": "20140912"}], "brand_name": "Ibuprofen", "product_id": "66715-9819_e5bf5e09-7d43-6314-e053-2a95a90a2325", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "66715-9819", "generic_name": "Ibuprofen tablet, film-coated", "labeler_name": "Lil' Drug Store Products, 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": "20140912", "listing_expiration_date": "20261231"}