Ibuprofen

Product NDC
69677-225
11-digit product format
696770225
Labeler code
69677
Product ID
69677-225_686b88b3-2ee0-3263-e053-2991aa0ac235
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mas Management Group, Inc.
Application
ANDA091625
Marketing category
ANDA
Marketing start
2015-12-21
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
600 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015Product name420230808
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69677-225-01Ibuprofen120 in 1 BOTTLETABLET, FILM COATED1202
69677-225-15Ibuprofen15 in 1 BOTTLETABLET, FILM COATED152
69677-225-20Ibuprofen20 in 1 BOTTLETABLET, FILM COATED202
69677-225-30Ibuprofen30 in 1 BOTTLETABLET, FILM COATED302
69677-225-60Ibuprofen60 in 1 BOTTLETABLET, FILM COATED602
69677-225-90Ibuprofen90 in 1 BOTTLETABLET, FILM COATED902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69677-225-01EA - Each69677-2255cbe2f02-4261-4efe-8816-8e01440e08c312017-10-13
69677-225-15EA - Each69677-2255b30fa75-bd96-40d1-b51f-12f8c7d9204f12017-10-13
69677-225-20EA - Each69677-225ce32baca-5836-4ab0-af83-b7d98ccceceb12017-10-13
69677-225-30EA - Each69677-2253d707e2e-d12a-4aa5-a107-b6dd5aa2a17712017-10-13
69677-225-60EA - Each69677-225ab8e3cf2-a68f-4832-a33f-eac8be7e29fc12017-10-13
69677-225-90EA - Each69677-225b0dfeee4-2ea1-46c5-aaa5-97fefa12218512017-10-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69677-225IBUPROFEN TABLET, FILM COATED [MAS MANAGEMENT GROUP, INC.]2Legacy NDC, 6 package rows20180328_57ec3a3f-b5ac-3a97-e053-2a91aa0a788f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197806ibuprofen 600 MG Oral TabletPSN57ec3a3f-b5ac-3a97-e053-2a91aa0a788f2
197807ibuprofen 800 MG Oral TabletPSN57ec3a3f-b5ac-3a97-e053-2a91aa0a788f2
197806ibuprofen 600 MG Oral TabletSCD57ec3a3f-b5ac-3a97-e053-2a91aa0a788f2
197807ibuprofen 800 MG Oral TabletSCD57ec3a3f-b5ac-3a97-e053-2a91aa0a788f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69677-225-0169677022501120 in 1 BOTTLEHistorical
69677-225-156967702251515 in 1 BOTTLEHistorical
69677-225-206967702252020 in 1 BOTTLEHistorical
69677-225-306967702253030 in 1 BOTTLEHistorical
69677-225-606967702256060 in 1 BOTTLEHistorical
69677-225-906967702259090 in 1 BOTTLEHistorical