FDA.reportPublic FDA data

NDC 70518-3466-01 - Propranolol Hydrochloride

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
70518-3466
Requested NDC
70518-3466-01
Package NDCs from labels
70518-3466-1, 70518-3466-0, 70518-3466-2, 70518-3466-3, 70518-3466-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-08-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Propranolol Hydrochloride - REMEDYREPACK INC.REMEDYREPACK INC.2026-08-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-3466-0Propranolol Hydrochloride100 in 1 BOXTABLET1009
70518-3466-1Propranolol Hydrochloride1 in 1 POUCHTABLET19
70518-3466-2Propranolol Hydrochloride30 in 1 BLISTER PACKTABLET309
70518-3466-3Propranolol Hydrochloride30 in 1 BLISTER PACKTABLET309

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-3466PROPRANOLOL HYDROCHLORIDE TABLET [REMEDYREPACK INC.]5Current NDC, Legacy NDC, 4 package rows20241006_a3bd3ef9-539d-450e-900b-95be0e46095b.zip

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 8 · 141 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
propranolol hydrochloridePROPRANOLOL HYDROCHLORIDEGolden State Medical Supply, Inc.5affa0ea-db84-86fd-e063-6294a90a4d162026-09-08Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEREMEDYREPACK INC.f7ae2dac-6048-41ea-95d3-cad06cc2baf32026-09-03Warnings, Adverse reactionsExact identifier
rxcui: 856519
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEAmerican Health Packagingc751ee54-27b4-4ed7-829a-ced735c413122026-09-02Warnings, Adverse reactionsExact identifier
rxcui: 856519
rxcui: 856457
rxcui: 856448
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEAmerican Health Packagingd027f39e-7648-44c8-a8dc-b26b4cdd81be2026-09-02Warnings, Adverse reactionsExact identifier
rxcui: 856519
rxcui: 856457
rxcui: 856448
unii: F8A3652H1V
Inderal XLPROPRANOLOL HYDROCHLORIDEANI Pharmaceuticals, Inc.ac196ff5-9215-402b-bc57-69aa87f8bade2026-08-27Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
InnoPran XLPROPRANOLOL HYDROCHLORIDEANI Pharmaceuticals, Inc.cd5601b3-4d87-4c3b-acac-b476e787609d2026-08-27Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
Propranolol Hydrochloride ERPROPRANOLOL HYDROCHLORIDEANI Pharmaceuticals, Inc.5415904b-90da-48e8-9f9e-f86749aa129c2026-08-27Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPar Health USA, LLC0d74bb04-8227-4afa-b523-ce1556150e072026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 856519
rxcui: 856578
rxcui: 856556
rxcui: 856457
rxcui: 856448
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPreferred Pharmaceuticals Inc.52da1afc-7f1c-4893-ab84-8479dd9399512026-08-24Warnings, Adverse reactionsExact identifier
rxcui: 856519
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPreferred Pharmaceuticals Inc.86c48c5a-0a59-43a7-b3b5-41ab5da72ce12026-08-24Warnings, Adverse reactionsExact identifier
rxcui: 856448
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPreferred Pharmaceuticals Inc.582fe781-0759-4622-8fa6-b7d90e94e6962026-08-24Warnings, Adverse reactionsExact identifier
rxcui: 856457
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPreferred Pharmaceuticals Inc.1791ef4d-b609-41c8-b4ef-15bff752ddd72026-08-24Warnings, Adverse reactionsExact identifier
application number: ANDA071972
rxcui: 856457
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPreferred Pharmaceuticals Inc.d9759182-e681-4c7e-af36-9f7b2184df3c2026-08-24Warnings, Adverse reactionsExact identifier
application number: ANDA071972
rxcui: 856448
unii: F8A3652H1V
INDERAL LAPROPRANOLOL HYDROCHLORIDEANI Pharmaceuticals, Inc.35d28979-36b1-4630-b85e-a44e0a4437342026-08-24Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDECreekwood Pharmaceuticals LLC289f39f4-ebd3-4fd9-bbb3-72de8124795a2026-08-21Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEREMEDYREPACK INC.a3bd3ef9-539d-450e-900b-95be0e46095b2026-08-10Warnings, Adverse reactionsExact identifier
application number: ANDA071972
ndc (package): 70518-3466-2
ndc (package): 70518-3466-0
ndc (package): 70518-3466-3
ndc (package): 70518-3466-1
ndc (product): 70518-3466
ndc11 (package): 70518346601
rxcui: 856457
spl id: 58b3340f-ee7b-8d3f-e063-6294a90af7a1
spl set id: a3bd3ef9-539d-450e-900b-95be0e46095b
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEPAI Holdings, LLC dba PAI Pharmafa5b6189-3419-4134-8bfe-c0d0c77df8282026-08-10Warnings, Adverse reactionsExact identifier
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEREMEDYREPACK INC.e3f615e0-07da-491c-9620-7083f4f4318a2026-08-07Warnings, Adverse reactionsExact identifier
application number: ANDA071972
rxcui: 856519
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEREMEDYREPACK INC.1cd914b6-b250-4b11-8404-41db3589361e2026-08-05Warnings, Adverse reactionsExact identifier
application number: ANDA071972
rxcui: 856448
unii: F8A3652H1V
Propranolol HydrochloridePROPRANOLOL HYDROCHLORIDEREMEDYREPACK INC.07c3fcab-33fe-4a6a-ba67-2d042190c1462026-08-04Warnings, Adverse reactionsExact identifier
rxcui: 856448
unii: F8A3652H1V

Reported adverse events (FAERS/openFDA)#

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