FDA.reportPublic FDA data

Ibuprofen and Pseudoephedrine hydrochloride

Product NDC
51660-493
11-digit product format
516600493
Labeler code
51660
Product ID
51660-493_f197efd7-d871-49e6-9984-51628bab7e8d
Type
HUMAN OTC DRUG
Nonproprietary name
ibuprofen and pseudoephedrine hydrochloride
Dosage form
TABLET, SUGAR COATED
Route
ORAL
Labeler
Ohm Laboratories Inc.
Application
ANDA074567
Marketing category
ANDA
Marketing start
2001-10-13
Substance
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Active strength
200; 30 mg/1; mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Ibuprofen and Pseudoephedrine hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IBUPROFEN200 mg/1
PSEUDOEPHEDRINE HYDROCHLORIDE30 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM, 6V9V2RYJ8N
Rxcui1299021

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
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
0fdb98e2-b951-a1ce-5715-2b187ba500efProduct name420170718
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
e974e22d-8688-7d92-1e87-40c1079e170cProduct name320151125
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
30c51294-7ae9-8007-7de6-58222684a0beProduct name120140508
4f26f669-fc6c-40ef-9e26-1c7b2390ee66Product name120140508
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
70a83adc-6047-bbea-5a08-dfd304aa47d2Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
858ce051-9941-aafc-8c7c-44a8e0227463Product name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508
b893258d-0942-3d8a-3411-056ea0788ff5Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51660-493-412020-09-10C16284748780-19d75b9d0-25a8-f424-e053-dadaa90a57ceIbuprofen and Pseudoephedrine hydrochloride
51660-493-412020-01-31C16284748780-19d75b9d0-25a8-f424-e053-dadaa90a57ceIbuprofen and Pseudoephedrine hydrochloride

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51660-493-41Ibuprofen and Pseudoephedrine hydrochloride40 in 1 BLISTER PACKTABLET, SUGAR COATED403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51660-493IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, SUGAR COATED [OHM LABORATORIES INC.]3Current NDC, Legacy NDC, 1 package rows20200911_cb7fb0d3-adf6-4c14-ac61-103dc869ebf2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1299021ibuprofen 200 MG / pseudoephedrine HCl 30 MG Oral TabletPSNcb7fb0d3-adf6-4c14-ac61-103dc869ebf23
1299021ibuprofen 200 MG / pseudoephedrine hydrochloride 30 MG Oral TabletSCDcb7fb0d3-adf6-4c14-ac61-103dc869ebf23

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
51660-493-415166004934140 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-493-41) 2001-10-130000-00-00NoNoCurrent