AUGMENTIN is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Dr. Reddy's Laboratories Inc. The primary component is Amoxicillin; Clavulanate Potassium.
| Product ID | 43598-021_81f11e22-8d19-4974-87d5-aa983d5ea945 |
| NDC | 43598-021 |
| Product Type | Human Prescription Drug |
| Proprietary Name | AUGMENTIN |
| Generic Name | Amoxicillin And Clavulanate Potassium |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1996-10-02 |
| Marketing Category | NDA / NDA |
| Application Number | NDA050720 |
| Labeler Name | Dr. Reddy's Laboratories Inc |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Active Ingredient Strength | 875 mg/1; 1/1 |
| Pharm 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 |
| Marketing Start Date | 1996-10-02 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA050720 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-10-02 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | NDA |
| Application Number | NDA050720 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-10-02 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| AMOXICILLIN | 875 mg/1 |
| SPL SET ID: | 174cc098-fe49-4f1a-87e2-601c7573f0db |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 72508-004 | AUGMENTIN | AUGMENTIN |
| 72508-006 | AUGMENTIN | AUGMENTIN |
| 72508-012 | AUGMENTIN | AUGMENTIN |
| 72508-021 | AUGMENTIN | AUGMENTIN |
| 72508-018 | AUGMENTIN | AUGMENTIN |
| 43598-004 | AUGMENTIN | AUGMENTIN |
| 43598-012 | AUGMENTIN | AUGMENTIN |
| 43598-021 | AUGMENTIN | AUGMENTIN |
| 43598-018 | AUGMENTIN | AUGMENTIN |
| 43598-006 | AUGMENTIN | AUGMENTIN |
| 61919-391 | AUGMENTIN | AUGMENTIN |
| 0093-2270 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0093-2272 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0093-2274 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0093-2275 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0093-2277 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0093-2279 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0093-8675 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0143-9249 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0143-9853 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0143-9981 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0143-9982 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0781-1619 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0781-1643 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0781-1831 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
| 0781-1852 | Amoxicillin and Clavulanate Potassium | Amoxicillin and Clavulanate Potassium |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AUGMENTIN 73746157 1533895 Dead/Cancelled |
BEECHAM INC. 1988-08-15 |
![]() AUGMENTIN 73195625 1144669 Live/Registered |
Beecham Inc. 1978-12-04 |