diclofenac sodium delayed release
Generic: diclofenac sodium
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
diclofenac sodium delayed release
Generic Name
diclofenac sodium
Labeler
a-s medication solutions
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
diclofenac sodium 75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7838
Product ID
50090-7838_8a5992ce-44cc-460a-970e-4d7b5ac068e5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075185
Listing Expiration
2026-12-31
Marketing Start
2025-03-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907838
Hyphenated Format
50090-7838
Supplemental Identifiers
RxCUI
UNII
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
diclofenac sodium delayed release (source: ndc)
Generic Name
diclofenac sodium (source: ndc)
Application Number
ANDA075185 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-0)
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-1)
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-2)
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-3)
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-4)
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-8)
- 180 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-9)
Packages (7)
50090-7838-0
100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-0)
50090-7838-1
20 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-1)
50090-7838-2
30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-2)
50090-7838-3
14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-3)
50090-7838-4
60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-4)
50090-7838-8
90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-8)
50090-7838-9
180 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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