FDA.reportPublic FDA data

Ibuprofen Sodium

Product NDC
0363-0909
11-digit product format
003630909
Labeler code
0363
Product ID
0363-0909_5dada37e-65d3-40b4-83ff-dbfc316e9f45
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Walgreen Company
Application
ANDA206581
Marketing category
ANDA
Marketing start
2016-01-13
Marketing end
0000-00-00
Substance
IBUPROFEN SODIUM
Active strength
256 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct0363-0909DDiscontinued by firm2026-07-31
excluded packagepackage0363-09090363-0909-27DDiscontinued by firm2026-07-31
excluded packagepackage0363-09090363-0909-49DDiscontinued by firm2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A206581-001IBUPROFEN SODIUMIBUPROFEN SODIUMEQ 200MG BASETABLET / ORAL2015-08-03

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A206581-001IBUPROFEN SODIUMEQ 200MG BASETABLET / ORAL2015-08-03a50c72e98297…

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0909-49EA - Each0363-090957f2ab07-9809-44bd-9990-7c6dd27f7bce12022-06-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-0909-27003630909271 BOTTLE in 1 CARTON (0363-0909-27) > 80 TABLET, FILM COATED in 1 BOTTLE1 bottle2016-01-130000-00-00NoNoCurrent
0363-0909-49003630909491 BOTTLE in 1 CARTON (0363-0909-49) > 40 TABLET, FILM COATED in 1 BOTTLE1 bottle2016-01-130000-00-00NoNoCurrent