motrin ib
Generic: ibuprofen
Labeler: lil' drug store products, inc.Drug Facts
Product Profile
Brand Name
motrin ib
Generic Name
ibuprofen
Labeler
lil' drug store products, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
66715-9812
Product ID
66715-9812_459bde25-f542-9aa4-e063-6394a90a6cb1
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA077349
Listing Expiration
2026-12-31
Marketing Start
2012-01-03
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
667159812
Hyphenated Format
66715-9812
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
motrin ib (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA077349 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 2 POUCH in 1 CARTON (66715-9812-2) / 2 TABLET, FILM COATED in 1 POUCH
- 3 POUCH in 1 CARTON (66715-9812-3) / 2 TABLET, FILM COATED in 1 POUCH
- 30 POUCH in 1 BOX, UNIT-DOSE (66715-9812-8) / 2 TABLET, FILM COATED in 1 POUCH
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459bde25-f542-9aa4-e063-6394a90a6cb1", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["201126", "310965"], "spl_set_id": ["c2b99756-3e03-4d9f-9ce6-7db879afe3a1"], "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": "2 POUCH in 1 CARTON (66715-9812-2) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-9812-2", "marketing_start_date": "20180618"}, {"sample": false, "description": "3 POUCH in 1 CARTON (66715-9812-3) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-9812-3", "marketing_start_date": "20190815"}, {"sample": false, "description": "30 POUCH in 1 BOX, UNIT-DOSE (66715-9812-8) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-9812-8", "marketing_end_date": "20280808", "marketing_start_date": "20220419"}], "brand_name": "Motrin IB", "product_id": "66715-9812_459bde25-f542-9aa4-e063-6394a90a6cb1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "66715-9812", "generic_name": "Ibuprofen", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motrin IB", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA077349", "marketing_category": "ANDA", "marketing_start_date": "20120103", "listing_expiration_date": "20261231"}