NDC 1500-0101 - OraVerse

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
1500-0101
Package NDCs from labels
1500-0101-01, 1500-0101-02
Manufacturer
Novalar Pharmaceuticals
Effective date
2008-05-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OraVerse - Novalar PharmaceuticalsNovalar Pharmaceuticals2008-05-23HUMAN PRESCRIPTION DRUG LABELING WITH HIGHLIGHTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
1500-0101-01OraVerse10 in 1 BLISTER PACKINJECTION, SOLUTION101
1500-0101-01OraVerse1 in 1 CARTONINJECTION, SOLUTION11
1500-0101-02OraVerse5 in 1 CARTONINJECTION, SOLUTION51
1500-0101-02OraVerse10 in 1 BLISTER PACKINJECTION, SOLUTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
1500-0101ORAVERSE (PHENTOLAMINE MESYLATE) INJECTION, SOLUTION FOR SUBMUCOSAL USE [NOVALAR PHARMACEUTICALS]14 package rows20080617_38be9414-87c4-4a8a-9f17-99be0d0a33fa.zip

DailyMed Socrata Ingredients#

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 1 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OraversePHENTOLAMINE MESYLATESeptodont, Inc.4025cf98-ea87-4531-b0fc-6283c84f63f32018-12-05Warnings, Adverse reactionsExact identifier
rxcui: 1361019
rxcui: 1361021
73841EBD-97FF-8476-B631-5A6F9A05AAFE38be9414-87c4-4a8a-9f17-99be0d0a33fa2008-05-23Warnings, Adverse reactionsExact identifier
spl id: 73841EBD-97FF-8476-B631-5A6F9A05AAFE
spl set id: 38be9414-87c4-4a8a-9f17-99be0d0a33fa

Reported adverse events (FAERS/openFDA)#

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