NDC 51552-0896-7

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: 51552-0896-7
Product root: 51552-0896
Identity scope: Package
Primary current NDC product row: Not present

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2022-04-09 23:13 UTC · source 2022-04-08	unfinished package	package	51552-0896	51552-0896-7	UNFINISHED	Active or certified unfinished drug listing		unfinished / ndc_unfinished.zip	`906f6e251498…`	`bf70b80e44f0…`
2021-12-27 23:28 UTC · source 2021-12-27	unfinished package	package	51552-0896	51552-0896-7	UNFINISHED	Active or certified unfinished drug listing		unfinished / ndc_unfinished.zip	`6db9cb8d1e19…`	`3449e1ec5b70…`

Reported adverse events (FAERS/openFDA)#

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