ibuprofen
Generic: ibuprofen
Labeler: safeway, inc.Drug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
safeway, inc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
21130-699
Product ID
21130-699_53e30a21-efc0-488c-b88a-9a35fcda3af7
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA078682
Listing Expiration
2027-12-31
Marketing Start
2021-05-28
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130699
Hyphenated Format
21130-699
Supplemental Identifiers
RxCUI
UPC
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
- 180 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (21130-699-18)
- 1 BOTTLE, PLASTIC in 1 BOX (21130-699-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (21130-699-30)
- 1 BOTTLE, PLASTIC in 1 BOX (21130-699-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 BOX (21130-699-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Packages (5)
21130-699-18
180 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (21130-699-18)
21130-699-20
1 BOTTLE, PLASTIC in 1 BOX (21130-699-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
21130-699-30
300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (21130-699-30)
21130-699-40
1 BOTTLE, PLASTIC in 1 BOX (21130-699-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
21130-699-80
1 BOTTLE, PLASTIC in 1 BOX (21130-699-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "53e30a21-efc0-488c-b88a-9a35fcda3af7", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0321130782315"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["57f06daf-690d-44a7-95a5-468732949750"], "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": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (21130-699-18)", "package_ndc": "21130-699-18", "marketing_end_date": "20270129", "marketing_start_date": "20210528"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-699-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-699-20", "marketing_start_date": "20210528"}, {"sample": false, "description": "300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (21130-699-30)", "package_ndc": "21130-699-30", "marketing_start_date": "20210528"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-699-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-699-40", "marketing_start_date": "20210528"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-699-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-699-80", "marketing_start_date": "20210528"}], "brand_name": "Ibuprofen", "product_id": "21130-699_53e30a21-efc0-488c-b88a-9a35fcda3af7", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-699", "generic_name": "Ibuprofen", "labeler_name": "Safeway, 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": "20210528", "listing_expiration_date": "20271231"}