NDC 71244-375

This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.

Requested NDC
71244-375
Product root
71244-375
Identity scope
Product
Primary current NDC product row
Not present

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 11 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
compounderpackage71244-37571244-375-20COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-24
compounderpackage71244-37571244-375-17COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-24
compounderpackage71244-37571244-375-15COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-24
compounderpackage71244-37571244-375-12COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-24
compounderpackage71244-37571244-375-10COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-24
compounderpackage71244-37571244-375-08COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-24
compounderpackage71244-37571244-375-17COMPOUNDEROutsourcing facility compounded drug report2019-12026-10-24
compounderpackage71244-37571244-375-12COMPOUNDEROutsourcing facility compounded drug report2019-12026-10-24
compounderpackage71244-37571244-375-08COMPOUNDEROutsourcing facility compounded drug report2019-12026-10-24
compounderpackage71244-37571244-375-15COMPOUNDEROutsourcing facility compounded drug report2019-12026-10-24
compounderpackage71244-37571244-375-20COMPOUNDEROutsourcing facility compounded drug report2019-12026-10-24

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 11 matching rows.

View current auxiliary records. · View the auxiliary file history.

Package NDC, Reporting period table
Package NDCReporting period
71244-375-082019-2
71244-375-202019-2
71244-375-152019-2
71244-375-172019-2
71244-375-102019-2
71244-375-122019-2
71244-375-172019-1
71244-375-122019-1
71244-375-202019-1
71244-375-152019-1
71244-375-082019-1

Compounder NDC reports#

Browse the complete compounder directory for this NDC · Browse every current compounder row in the unified auxiliary catalog · browse compounder source captures and parsed snapshots.

Establishment, FEI, Product NDC table
EstablishmentFEIProduct NDCPackage NDCProductActive ingredientsReporting periodNormalization
"Pentec Health, Inc(080215699)"71244-37571244-375-08Vancomycin Hydrochloride100 mg/1 mL2019-2valid
"Pentec Health, Inc(080215699)"71244-37571244-375-10Vancomycin Hydrochloride100 mg/1 mL2019-2valid
"Pentec Health, Inc(080215699)"71244-37571244-375-12Vancomycin Hydrochloride100 mg/1 mL2019-2valid
"Pentec Health, Inc(080215699)"71244-37571244-375-15Vancomycin Hydrochloride100 mg/1 mL2019-2valid
"Pentec Health, Inc(080215699)"71244-37571244-375-17Vancomycin Hydrochloride100 mg/1 mL2019-2valid
"Pentec Health, Inc(080215699)"71244-37571244-375-20Vancomycin Hydrochloride100 mg/1 mL2019-2valid
"Pentec Health, Inc(080215699)"71244-37571244-375-08Vancomycin Hydrochloride100 mg/1 mL2019-1valid
"Pentec Health, Inc(080215699)"71244-37571244-375-12Vancomycin Hydrochloride100 mg/1 mL2019-1valid
"Pentec Health, Inc(080215699)"71244-37571244-375-15Vancomycin Hydrochloride100 mg/1 mL2019-1valid
"Pentec Health, Inc(080215699)"71244-37571244-375-17Vancomycin Hydrochloride100 mg/1 mL2019-1valid
"Pentec Health, Inc(080215699)"71244-37571244-375-20Vancomycin Hydrochloride100 mg/1 mL2019-1valid

Reported adverse events (FAERS/openFDA)#

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