ibuprofen
Generic: ibuprofen
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
cvs pharmacy, inc.
Dosage Form
TABLET
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-391
Product ID
69842-391_71d1d56e-b34c-430b-a083-f305487ebfe6
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA079174
Listing Expiration
2026-12-31
Marketing Start
2017-11-09
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842391
Hyphenated Format
69842-391
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
ANDA079174 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 15 POUCH in 1 CARTON (69842-391-54) / 2 TABLET in 1 POUCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "71d1d56e-b34c-430b-a083-f305487ebfe6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["cdd5a402-df90-4a16-a38c-78eab7189998"], "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": ["CVS PHARMACY, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 POUCH in 1 CARTON (69842-391-54) / 2 TABLET in 1 POUCH", "package_ndc": "69842-391-54", "marketing_start_date": "20171109"}], "brand_name": "Ibuprofen", "product_id": "69842-391_71d1d56e-b34c-430b-a083-f305487ebfe6", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69842-391", "generic_name": "Ibuprofen", "labeler_name": "CVS PHARMACY, 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": "20171109", "listing_expiration_date": "20261231"}