FDA.reportPublic FDA data

NDC 60219-1752-01 - 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
60219-1752
Requested NDC
60219-1752-01
Package NDCs from labels
60219-1752-3, 60219-1752-1, 60219-1752-7, 60219-1752-01
Manufacturer
Bryant Ranch Prepack
Effective date
2026-08-11
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 Prepack2026-08-11HUMAN PRESCRIPTION DRUG LABEL
Sildenafil - Amneal Pharmaceuticals NY LLCAmneal Pharmaceuticals NY LLC2026-07-06HUMAN PRESCRIPTION DRUG LABEL
Sildenafil - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2023-09-20HUMAN PRESCRIPTION DRUG LABEL
Sildenafil - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2022-12-07HUMAN PRESCRIPTION DRUG LABEL
Sildenafil - A-S Medication SolutionsA-S Medication Solutions2021-04-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60219-1752-1Sildenafil100 in 1 BOTTLETABLET, FILM COATED10012
60219-1752-3Sildenafil30 in 1 BOTTLETABLET, FILM COATED3012
60219-1752-7Sildenafil1000 in 1 BOTTLETABLET, FILM COATED100012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60219-1752SILDENAFIL 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
60219-1752-3EA - Each60219-1752993a8875-3915-4006-a9d4-028368f95da612018-09-05

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 9 · 166 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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
SildenafilSILDENAFILPreferred Pharmaceuticals Inc.d887377e-90c5-44dc-8455-b23a6755b36f2026-08-28Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
SildenafilSILDENAFILBryant Ranch Prepack96ae6733-cef9-46cf-bf4e-5368201943bd2026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA202023
rxcui: 314229
unii: BW9B0ZE037
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
ndc (package): 63629-7833-7
ndc (package): 63629-7833-6
ndc (package): 63629-7833-3
ndc (package): 63629-7833-2
ndc (package): 63629-7833-8
ndc (package): 63629-7833-4
ndc (package): 63629-7833-1
ndc (package): 63629-7833-5
ndc (product): 63629-7833
rxcui: 312950
spl id: fd77efe1-6233-489b-838c-aa3c9cf9d3f5
spl set id: dfe4f616-b5de-458c-a97b-ab860e32320c
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
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
SildenafilSILDENAFIL CITRATEYaral Pharma Inc.a17a970e-25a2-4807-9644-74e6d2bd23832026-07-17Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
SildenafilSILDENAFILAmneal Pharmaceuticals LLC187de471-3e79-44ed-b560-0f8b2d549f742026-07-16Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
SildenafilSILDENAFILREMEDYREPACK INC.99bc66a4-05d1-4372-a25a-1153d7af580e2026-07-14Warnings, Adverse reactionsExact identifier
rxcui: 312950
unii: BW9B0ZE037
SildenafilSILDENAFILREMEDYREPACK INC.e4f41e9e-d508-4f91-8677-8a19b07139de2026-07-09Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
VybriqueSILDENAFIL CITRATEIBSA Pharma Inc.9213fec1-e0c0-4ef7-9718-d97922a3f4d82026-07-08Warnings, Adverse reactionsExact identifier
unii: BW9B0ZE037
SildenafilSILDENAFILPD-Rx Pharmaceuticals, Inc.e1af7b6a-378e-4337-858f-85a926eec1022026-07-07Warnings, Adverse reactionsExact identifier
rxcui: 314229
unii: BW9B0ZE037
SildenafilSILDENAFILPD-Rx Pharmaceuticals, Inc.4e3034af-bee5-4df4-8beb-fbd2b510ad732026-07-07Warnings, Adverse reactionsExact identifier
rxcui: 312950
unii: BW9B0ZE037
SildenafilSILDENAFILAmneal Pharmaceuticals NY LLCa1c3a2a2-8cf5-41c3-9c86-54290570d9162026-07-06Warnings, Adverse reactionsExact identifier
application number: ANDA202023
ndc (package): 60219-1752-7
ndc (package): 60219-1752-3
ndc (package): 60219-1753-1
ndc (package): 60219-1751-3
ndc (package): 60219-1753-7
ndc (package): 60219-1751-1
ndc (package): 60219-1751-7
ndc (package): 60219-1752-1
ndc (package): 60219-1753-3
ndc (product): 60219-1752
ndc (product): 60219-1751
ndc (product): 60219-1753
ndc11 (package): 60219175201
rxcui: 314229
rxcui: 312950
rxcui: 314228
spl id: 64d4569d-26f0-4120-bc1e-c8dc47dcb387
spl set id: a1c3a2a2-8cf5-41c3-9c86-54290570d916
unii: BW9B0ZE037

Reported adverse events (FAERS/openFDA)#

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