infants ibuprofen
Generic: ibuprofen
Labeler: safewayDrug Facts
Product Profile
Brand Name
infants ibuprofen
Generic Name
ibuprofen
Labeler
safeway
Dosage Form
SUSPENSION/ DROPS
Routes
Active Ingredients
ibuprofen 50 mg/1.25mL
Manufacturer
Identifiers & Regulatory
Product NDC
21130-513
Product ID
21130-513_f1f80214-006b-462f-a825-babb6cde97f4
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA075217
Listing Expiration
2026-12-31
Marketing Start
2025-06-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130513
Hyphenated Format
21130-513
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
infants ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA075217 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1.25mL
Packaging
- 1 BOTTLE in 1 CARTON (21130-513-10) / 30 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f1f80214-006b-462f-a825-babb6cde97f4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["204442"], "spl_set_id": ["6fed7c65-69a3-4899-a85d-23ea95f571a4"], "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"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-513-10) / 30 mL in 1 BOTTLE", "package_ndc": "21130-513-10", "marketing_start_date": "20250618"}], "brand_name": "INFANTS IBUPROFEN", "product_id": "21130-513_f1f80214-006b-462f-a825-babb6cde97f4", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-513", "generic_name": "Ibuprofen", "labeler_name": "Safeway", "product_type": "HUMAN OTC DRUG", "brand_name_base": "INFANTS IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "50 mg/1.25mL"}], "application_number": "ANDA075217", "marketing_category": "ANDA", "marketing_start_date": "20250618", "listing_expiration_date": "20261231"}