FDA.reportPublic FDA data

Sildenafil

Product NDC
68071-4517
11-digit product format
680714517
Labeler code
68071
Product ID
68071-4517_1ab3529e-7ae6-bf8a-e063-6294a90a6fcb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sildenafil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA203814
Marketing category
ANDA
Marketing start
2014-01-03
Marketing end
2027-10-31
Substance
SILDENAFIL CITRATE
Active strength
20 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sildenafil

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILDENAFIL CITRATE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiBW9B0ZE037
Rxcui577033

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fabccea2-36c8-9268-ee44-ec231455538fProduct name920241217
ac996ae9-22a2-41c2-bb86-913c4aef95adProduct name120230606
fc95c9f0-00dc-40ef-bcea-b60c9009c5fcProduct name920220613

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4517-92024-06-12C16284748780-1ba0f9c33-3d08-a910-e053-dadaa90a0b85These highlights do not include all the information needed to use sildenafil tablets safely and effectively. See full prescribing information for sildenafil tablets. SILDENAFIL tablets, for oral use. Initial U.S. Approval: 1998
68071-4517-92023-01-30C16284748780-1ba0f9c33-3d08-a910-e053-dadaa90a0b85These highlights do not include all the information needed to use sildenafil tablets safely and effectively. See full prescribing information for sildenafil tablets. SILDENAFIL tablets, for oral use. Initial U.S. Approval: 1998
68071-4517-92021-02-19C16284748780-1ba0f9c33-3d08-a910-e053-dadaa90a0b85These highlights do not include all the information needed to use sildenafil tablets safely and effectively. See full prescribing information for sildenafil tablets. SILDENAFIL tablets, for oral use. Initial U.S. Approval: 1998
68071-4517-92021-01-29C16284748780-1ba0f9c33-3d08-a910-e053-dadaa90a0b85These highlights do not include all the information needed to use sildenafil tablets safely and effectively. See full prescribing information for sildenafil tablets. SILDENAFIL tablets, for oral use. Initial U.S. Approval: 1998

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-4517-9Sildenafil90 in 1 BOTTLETABLET, FILM COATED905

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-4517SILDENAFIL TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.]5Current NDC, Legacy NDC, 1 package rows20240613_72900ed9-dbab-3f7b-e053-2a91aa0a0d24.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
577033sildenafil citrate 20 MG Oral TabletPSN72900ed9-dbab-3f7b-e053-2a91aa0a0d245
577033sildenafil 20 MG Oral TabletSCD72900ed9-dbab-3f7b-e053-2a91aa0a0d245
577033sildenafil 20 MG (as sildenafil citrate) Oral TabletSY72900ed9-dbab-3f7b-e053-2a91aa0a0d245

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68071-4517-96807145170990 TABLET, FILM COATED in 1 BOTTLE (68071-4517-9) 2018-08-032027-10-31NoNoCurrent