FDA.reportPublic FDA data

NDC 60219-1753-01 - Sildenafil

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
60219-1753
Requested NDC
60219-1753-01
Package NDCs from labels
60219-1753-3, 60219-1753-1, 60219-1753-7, 60219-1753-01
Manufacturer
Bryant Ranch Prepack
Effective date
2026-08-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sildenafil - Bryant Ranch PrepackBryant Ranch Prepack2026-08-19HUMAN PRESCRIPTION DRUG LABEL
Sildenafil - Amneal Pharmaceuticals NY LLCAmneal Pharmaceuticals NY LLC2026-07-06HUMAN PRESCRIPTION DRUG LABEL
Sildenafil - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2025-02-10HUMAN PRESCRIPTION DRUG LABEL
Tadalafil - CarePartners Pharmacy, LLCCarePartners Pharmacy, LLC2019-08-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60219-1753-1Sildenafil100 in 1 BOTTLETABLET, FILM COATED10012
60219-1753-3Sildenafil30 in 1 BOTTLETABLET, FILM COATED3012
60219-1753-7Sildenafil1000 in 1 BOTTLETABLET, FILM COATED100012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60219-1753SILDENAFIL TABLET, FILM COATED [AMNEAL PHARMACEUTICALS NY LLC]12Current NDC, Legacy NDC, 3 package rows20231128_a1c3a2a2-8cf5-41c3-9c86-54290570d916.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60219-1753-3EA - Each60219-17537a949024-1edd-451b-85cf-2f18ae1c672c12018-09-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 16 · 309 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TadalafilTADALAFILA-S Medication Solutionsb1840f16-a7ea-44bd-b091-5268990aedb22026-09-09Warnings, Adverse reactionsExact identifier
rxcui: 402019
unii: 742SXX0ICT
TadalafilTADALAFILA-S Medication Solutions81222924-29d9-4031-954d-132923867b8e2026-09-09Warnings, Adverse reactionsExact identifier
rxcui: 402019
unii: 742SXX0ICT
SildenafilSILDENAFILPreferred Pharmaceuticals, Inc.174ef537-e3e6-42bd-a478-47b930ddc7612026-08-31Warnings, Adverse reactionsExact identifier
rxcui: 314229
unii: BW9B0ZE037
Sildenafil CitrateSILDENAFILPreferred Pharmaceuticals Inc.878b4c44-cddc-42cb-b9b5-911451ad15302026-08-31Warnings, Adverse reactionsExact identifier
rxcui: 314229
unii: BW9B0ZE037
TadalafilTADALAFILA-S Medication Solutionscf9431ef-ea02-457d-b83a-ce13fb963d952026-08-28Warnings, Adverse reactionsExact identifier
rxcui: 402019
unii: 742SXX0ICT
SildenafilSILDENAFILPreferred Pharmaceuticals Inc.d887377e-90c5-44dc-8455-b23a6755b36f2026-08-28Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
tadalafilTADALAFILBryant Ranch Prepack394be6ef-c0f7-4cd5-8062-39fda5c1c2c42026-08-27Warnings, Adverse reactionsExact identifier
application number: ANDA209250
rxcui: 484814
unii: 742SXX0ICT
TadalafilTADALAFILA-S Medication Solutionsa6847ad6-3b5b-47e5-a3b5-04dc3182d72b2026-08-25Warnings, Adverse reactionsExact identifier
rxcui: 402019
unii: 742SXX0ICT
SildenafilSILDENAFILBryant Ranch Prepack96ae6733-cef9-46cf-bf4e-5368201943bd2026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA202023
ndc (package): 71335-0969-5
ndc (package): 71335-0969-6
ndc (package): 71335-0969-9
ndc (package): 71335-0969-1
ndc (package): 71335-0969-4
ndc (package): 71335-0969-0
ndc (package): 71335-0969-8
ndc (package): 71335-0969-2
ndc (package): 71335-0969-3
ndc (package): 71335-0969-7
ndc (product): 71335-0969
rxcui: 314229
spl id: 1621566d-9ec1-4b85-a5ac-247044d9f9d1
spl set id: 96ae6733-cef9-46cf-bf4e-5368201943bd
unii: BW9B0ZE037
TadalafilTADALAFILNuCare Pharmaceuticals,Inc.c3409762-3b2b-1cfc-e053-2995a90ab91b2026-08-18Warnings, Adverse reactionsExact identifier
rxcui: 402019
unii: 742SXX0ICT
SILDENAFILSILDENAFILCardinal Health 107, LLCc5ac2265-393a-4fbe-b974-1dd0b9243ec82026-08-12Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
Sildenafil CitrateSILDENAFILNuCare Pharmaceuticals,Inc.1b1ab00d-de9c-4614-e063-6394a90afcde2026-08-11Warnings, Adverse reactionsExact identifier
rxcui: 312950
unii: BW9B0ZE037
SildenafilSILDENAFILBryant Ranch Prepackdfe4f616-b5de-458c-a97b-ab860e32320c2026-08-11Warnings, Adverse reactionsExact identifier
application number: ANDA202023
rxcui: 312950
unii: BW9B0ZE037
SildenafilSILDENAFILA-S Medication Solutionsdc38f412-dca7-4b54-b14c-314e7a251ee62026-08-10Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
SildenafilSILDENAFILBryant Ranch Prepacka636d3c7-af25-4148-8b4e-6f44deba700b2026-08-06Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
SildenafilSILDENAFILJubilant Cadista Pharmaceuticals Inc.1ed2420b-478a-ca9c-0330-85c845acdd322026-08-03Warnings, Adverse reactionsExact identifier
rxcui: 314229
rxcui: 312950
rxcui: 314228
unii: BW9B0ZE037
TadalafilTADALAFILNuCare Pharmaceuticals,Inc.d6e8c52f-4dc3-5d54-e053-2995a90a93582026-08-03Warnings, Adverse reactionsExact identifier
rxcui: 402019
unii: 742SXX0ICT
TadalafilTADALAFILNorthStar Rx, LLCa10d464a-6ea7-4e5a-befa-71eceacc50392026-07-30Warnings, Adverse reactionsExact identifier
rxcui: 402019
rxcui: 403957
rxcui: 757707
rxcui: 484814
unii: 742SXX0ICT
SILDENAFIL CITRATESILDENAFIL CITRATEPD-Rx Pharmaceuticals, Inc.00ee09dd-2de0-4dc4-85f6-b51ed6eabd5b2026-07-29Warnings, Adverse reactionsExact identifier
rxcui: 314228
unii: BW9B0ZE037
SILDENAFIL CITRATESILDENAFIL CITRATEPD-Rx Pharmaceuticals, Inc.f1122baa-8dee-43fc-bd3d-501a55b696b32026-07-29Warnings, Adverse reactionsExact identifier
rxcui: 314229
unii: BW9B0ZE037

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.