Home NDC 43598-021 AUGMENTIN
Product NDC 43598-021
11-digit product format 435980021
Labeler code 43598
Product ID 43598-021_81f11e22-8d19-4974-87d5-aa983d5ea945
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name amoxicillin and clavulanate potassium
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Dr. Reddy's Laboratories Inc
Application NDA050720
Marketing category NDA
Marketing start 1996-10-02
Marketing end 0000-00-00
Substance AMOXICILLIN; CLAVULANATE POTASSIUM
Active strength 875 mg/1; 1/1
Pharmacologic classes Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
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 2 · 66 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
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 N050720-001 AUGMENTIN '875' AMOXICILLIN; CLAVULANATE POTASSIUM 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code N050720-001 AB
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 2 · 43 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 2026-09-14 22:38:34 2026-08 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 84e616aacf4f…2026-08-18 06:07:40 2026-07 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 87673890dc5c…2021-03-12 10:30 UTC 2021-03 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 3f01610625f2…2019-09-15 20:21 UTC 2019-09 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 b00525d2431f…2019-07-19 19:46 UTC 2019-07 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 053a50430f4f…2023-01-26 05:58 UTC 2023-01 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 N050720-001 AUGMENTIN '875' 875MG;EQ 125MG BASE TABLET / ORAL AB RLD 1996-02-13 f41ea6bd6efb…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 43 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 43598-021-14 AUGMENTIN 20 in 1 BOTTLE TABLET, FILM COATED 20 6 43598-021-78 AUGMENTIN 100 in 1 BOX, UNIT-DOSE TABLET, FILM COATED 100 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded AMOXICILLIN ACTIVE INGREDIENT 804826J2HU AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 CLAVULANATE POTASSIUM ACTIVE INGREDIENT Q42OMW3AT8 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 AMOXICILLIN ANHYDROUS ACTIVE MOIETY 9EM05410Q9 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 CLAVULANIC ACID ACTIVE MOIETY 23521W1S24 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 ASPARTAME INACTIVE INGREDIENT Z0H242BBR1 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 MANNITOL INACTIVE INGREDIENT 3OWL53L36A AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 SACCHARIN SODIUM DIHYDRATE INACTIVE INGREDIENT SB8ZUX40TY AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43598-021 AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, FILM COATED AUGMENTIN (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION [DR. REDDY'S LABORATORIES INC] 6 Legacy NDC, 2 package rows 20160913_174cc098-fe49-4f1a-87e2-601c7573f0db.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 · 3 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 43598-021-14 43598002114 20 in 1 BOTTLE Historical 43598-021-78 43598002178 100 in 1 BOX, UNIT-DOSE Historical