Sildenafil

Product NDC
68071-2608
11-digit product format
680712608
Labeler code
68071
Product ID
68071-2608_d462e818-af96-0b23-e053-2995a90ace22
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sildenafil
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA210394
Marketing category
ANDA
Marketing start
2018-05-04
Marketing end
0000-00-00
Substance
SILDENAFIL CITRATE
Active strength
20 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-2608-3Sildenafil30 in 1 BOTTLETABLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-2608SILDENAFIL TABLET [NUCARE PHARMACEUTICALS,INC.]3Legacy NDC, 1 package rows20230715_d462e818-af97-0b23-e053-2995a90ace22.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
577033sildenafil citrate 20 MG Oral TabletPSNd462e818-af97-0b23-e053-2995a90ace223
577033sildenafil 20 MG Oral TabletSCDd462e818-af97-0b23-e053-2995a90ace223
577033sildenafil 20 MG (as sildenafil citrate) Oral TabletSYd462e818-af97-0b23-e053-2995a90ace223

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-2608-36807126080330 TABLET in 1 BOTTLE (68071-2608-3) 30 tablet2021-12-300000-00-00NoNoCurrent