ibuprofen oral
Generic: ibuprofen oral
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ibuprofen oral
Generic Name
ibuprofen oral
Labeler
a-s medication solutions
Dosage Form
SUSPENSION
Routes
Active Ingredients
ibuprofen 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4129
Product ID
50090-4129_ab18686c-599d-47b2-863a-1f9c6c0c42f9
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA210602
Listing Expiration
2026-12-31
Marketing Start
2018-11-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904129
Hyphenated Format
50090-4129
Supplemental Identifiers
RxCUI
UNII
NUI
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 oral (source: ndc)
Generic Name
ibuprofen oral (source: ndc)
Application Number
ANDA210602 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (50090-4129-0) / 118 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": "ab18686c-599d-47b2-863a-1f9c6c0c42f9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["a8672e5a-61f2-46d8-9401-432a978d2fd3"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-4129-0) / 118 mL in 1 BOTTLE", "package_ndc": "50090-4129-0", "marketing_start_date": "20190207"}], "brand_name": "Ibuprofen Oral", "product_id": "50090-4129_ab18686c-599d-47b2-863a-1f9c6c0c42f9", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-4129", "generic_name": "Ibuprofen Oral", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen Oral", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA210602", "marketing_category": "ANDA", "marketing_start_date": "20181123", "listing_expiration_date": "20261231"}