Application 050762

Type: NDA
Sponsor: PFIZER

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	TROVAN/ZITHROMAX COMPLIANCE PAK	AZITHROMYCIN DIHYDRATE; TROVAFLOXACIN MESYLATE	FOR SUSPENSION, TABLET;ORAL	EQ 1GM BASE,N/A;N/A,EQ 100MG BASE	No	No

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N050762-001	TROVAN/ZITHROMAX COMPLIANCE PAK	AZITHROMYCIN DIHYDRATE; TROVAFLOXACIN MESYLATE	EQ 1GM BASE,N/A;N/A,EQ 100MG BASE	FOR SUSPENSION, TABLET / ORAL			1998-12-18

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 2 of 2 · 44 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2022-10-28 04:53 UTC	2022-10	N050762-001	TROVAN/ZITHROMAX COMPLIANCE PAK	EQ 1GM BASE,N/A;N/A,EQ 100MG BASE	FOR SUSPENSION, TABLET / ORAL	1998-12-18	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	N050762-001	TROVAN/ZITHROMAX COMPLIANCE PAK	EQ 1GM BASE,N/A;N/A,EQ 100MG BASE	FOR SUSPENSION, TABLET / ORAL	1998-12-18	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	N050762-001	TROVAN/ZITHROMAX COMPLIANCE PAK	EQ 1GM BASE,N/A;N/A,EQ 100MG BASE	FOR SUSPENSION, TABLET / ORAL	1998-12-18	`cb3db0bc1861…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	N050762-001	TROVAN/ZITHROMAX COMPLIANCE PAK	EQ 1GM BASE,N/A;N/A,EQ 100MG BASE	FOR SUSPENSION, TABLET / ORAL	1998-12-18	`a50c72e98297…`

Reported adverse events (FAERS/openFDA)#

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

Documents#

Document, Submission type, Date table
Document	Submission type	Date
42728	ORIG	1999-07-04
8243	ORIG	1998-12-28
39301	ORIG	1998-12-18