FDA.reportPublic FDA data

NDC 72542-002 - OLPRUVA

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
72542-002
Package NDCs from labels
72542-002-01
Manufacturer
Acer Therapeutics Inc. | CH Chemie Uetikon GmbH | EMSL Analytical, Inc. DBA MPL Laboratories | Glatt Air Techniques Inc. | Sharp Clinical Services LLC
Effective date
2024-12-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OLPRUVAAcer Therapeutics Inc. | CH Chemie Uetikon GmbH | EMSL Analytical, Inc. DBA MPL Laboratories | Glatt Air Techniques Inc. | Sharp Clinical Services LLC2024-12-18HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72542-002-01OLPRUVA1 in 1 PACKETFOR SUSPENSION22 g4
72542-002-01OLPRUVA1 in 1 PACKETFOR SUSPENSION12 g4
72542-002-01OLPRUVA1 in 1 PACKETFOR SUSPENSION12 g4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72542-002OLPRUVA (SODIUM PHENYLBUTYRATE) KIT [ACER THERAPEUTICS INC.]4Unmatched20241220_89abc31c-43e8-4809-9eb7-172cb31a86f1.zip