ibuprofen
Generic: ibuprofen
Labeler: chain drug marketing association, inc.Drug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
chain drug marketing association, inc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63868-470
Product ID
63868-470_f0d3a221-4870-abc3-e053-2995a90aa4be
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA078682
Listing Expiration
2026-12-31
Marketing Start
2019-10-09
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868470
Hyphenated Format
63868-470
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
ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA078682 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (63868-470-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (63868-470-48) / 48 CAPSULE, LIQUID FILLED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (63868-470-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f0d3a221-4870-abc3-e053-2995a90aa4be", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["553d16e1-928e-4919-bc53-6683a035e2b0"], "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": ["Chain Drug Marketing Association, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63868-470-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "63868-470-20", "marketing_start_date": "20191009"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (63868-470-48) / 48 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "63868-470-48", "marketing_start_date": "20191009"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (63868-470-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "63868-470-80", "marketing_start_date": "20191009"}], "brand_name": "Ibuprofen", "product_id": "63868-470_f0d3a221-4870-abc3-e053-2995a90aa4be", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63868-470", "generic_name": "Ibuprofen", "labeler_name": "Chain Drug Marketing Association, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA078682", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}