Home NDC 55695-029 azithromycin
Product NDC 55695-029
11-digit product format 556950029
Labeler code 55695
Product ID 55695-029_2e0577d5-adb9-6c8d-e054-00144ff8d46c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name azithromycin
Dosage form POWDER, FOR SUSPENSION
Route ORAL
Labeler Department of State Health Services, Pharmacy Branch
Application NDA050710
Marketing category NDA AUTHORIZED GENERIC
Marketing start 1995-10-19
Marketing end 0000-00-00
Substance AZITHROMYCIN DIHYDRATE
Active strength 900 mg/22.5mL
Pharmacologic classes Macrolide Antimicrobial [EPC],Macrolides [CS]
NDC exclude flag E
Listing certified through 2018-12-31
Current FDA listing Historical FDA.report record 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 · 44 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 55695-029-00 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 55695-029-00 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 55695-029-00 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 55695-029-00 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 55695-029-00 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 55695-029-00 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 55695-029-00 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 55695-029-00 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 55695-029-00 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 55695-029-00 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 55695-029-00 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 55695-029-00 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 55695-029-00 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 55695-029-00 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 55695-029-00 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 55695-029-00 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 55695-029-00 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 55695-029-00 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 55695-029-00 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 55695-029-00 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 55695-029-00 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 55695-029-00 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N050710-001 ZITHROMAX AZITHROMYCIN EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 N050710-002 ZITHROMAX AZITHROMYCIN EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
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 1 of 3 · 82 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 bb7c543d1eb4…2022-03-09 01:35 UTC 2022-03 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 N050710-001 ZITHROMAX EQ 100MG BASE/5ML FOR SUSPENSION / ORAL AB RLD 1995-10-19 782e0a99824c…2021-12-28 21:50 UTC 2021-12 N050710-002 ZITHROMAX EQ 200MG BASE/5ML FOR SUSPENSION / ORAL AB RLD, RS 1995-10-19 782e0a99824c…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 82 observed states.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55695-029-00 azithromycin 22.5 mL in 1 BOTTLE POWDER, FOR SUSPENSION 22.5 2 55695-029-00 azithromycin 1 in 1 CARTON POWDER, FOR SUSPENSION 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55695-029 AZITHROMYCIN TABLET, FILM COATED AZITHROMYCIN POWDER, FOR SUSPENSION [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] 2 Legacy NDC, 2 package rows 20160314_2dc92556-ca5a-608c-e054-00144ff88e88.zip
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 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Zithromax AZITHROMYCIN DIHYDRATE Pfizer Laboratories Div Pfizer Inc db52b91e-79f7-4cc1-9564-f2eee8e31c45 2026-07-24 Warnings, Adverse reactions Exact identifier application applno (NDA): 050710 application number: NDA050710
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 55695-029-00 55695002900 22.5 mL in 1 BOTTLE 22.5 ml Historical