ibuprofen
Generic: ibuprofen
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7288
Product ID
50090-7288_73a943cb-930a-4bed-9fa6-f818926e2e7a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202413
Listing Expiration
2026-12-31
Marketing Start
2024-05-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907288
Hyphenated Format
50090-7288
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 (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA202413 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 600 mg/1
Packaging
- 10 TABLET, FILM COATED in 1 BOTTLE (50090-7288-0)
- 16 TABLET, FILM COATED in 1 BOTTLE (50090-7288-2)
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-7288-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (50090-7288-4)
- 100 TABLET, FILM COATED in 1 BOTTLE (50090-7288-5)
- 40 TABLET, FILM COATED in 1 BOTTLE (50090-7288-7)
- 20 TABLET, FILM COATED in 1 BOTTLE (50090-7288-8)
- 24 TABLET, FILM COATED in 1 BOTTLE (50090-7288-9)
Packages (8)
50090-7288-0
10 TABLET, FILM COATED in 1 BOTTLE (50090-7288-0)
50090-7288-2
16 TABLET, FILM COATED in 1 BOTTLE (50090-7288-2)
50090-7288-3
30 TABLET, FILM COATED in 1 BOTTLE (50090-7288-3)
50090-7288-4
60 TABLET, FILM COATED in 1 BOTTLE (50090-7288-4)
50090-7288-5
100 TABLET, FILM COATED in 1 BOTTLE (50090-7288-5)
50090-7288-7
40 TABLET, FILM COATED in 1 BOTTLE (50090-7288-7)
50090-7288-8
20 TABLET, FILM COATED in 1 BOTTLE (50090-7288-8)
50090-7288-9
24 TABLET, FILM COATED in 1 BOTTLE (50090-7288-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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