Amoxicillin and Clavulanate Potassium
- Product NDC
- 53002-7891
- 11-digit product format
- 530027891
- Labeler code
- 53002
- Product ID
- 53002-7891_8d6b454b-61eb-4e4f-abc3-30e47f414d23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amoxicillin and clavulanate potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA065093
- Marketing category
- ANDA
- Marketing start
- 2002-11-21
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875 mg/1; mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 53002-7891-2 | 2025-01-30 | C162847 | 48780-1 | 9d75b9d0-a18f-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use amoxicillin and clavulanate potassium safely and effectively. See full prescribing information for AMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS, and AMOXICILLIN AND CLAVULANATE POTASSIUM FOR ORAL SUSPENSION. AMOXICILLIN and CLAVULANATE potassium tablets, and AMOXICILLIN and CLAVULANATE potassium for oral suspension, for oral use Initial U.S. Approval: 1984 |
| 53002-7891-2 | 2023-06-07 | C162847 | 48780-1 | 9d75b9d0-a18f-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use amoxicillin and clavulanate potassium safely and effectively. See full prescribing information for AMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS, and AMOXICILLIN AND CLAVULANATE POTASSIUM FOR ORAL SUSPENSION. AMOXICILLIN and CLAVULANATE potassium tablets, and AMOXICILLIN and CLAVULANATE potassium for oral suspension, for oral use Initial U.S. Approval: 1984 |
| 53002-7891-2 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d0-a18f-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use amoxicillin and clavulanate potassium safely and effectively. See full prescribing information for AMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS, and AMOXICILLIN AND CLAVULANATE POTASSIUM FOR ORAL SUSPENSION. AMOXICILLIN and CLAVULANATE potassium tablets, and AMOXICILLIN and CLAVULANATE potassium for oral suspension, for oral use Initial U.S. Approval: 1984 |
| 53002-7891-2 | 2020-12-15 | C162847 | 48780-1 | 9d75b9d0-a18f-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use amoxicillin and clavulanate potassium safely and effectively. See full prescribing information for AMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS, and AMOXICILLIN AND CLAVULANATE POTASSIUM FOR ORAL SUSPENSION. AMOXICILLIN and CLAVULANATE potassium tablets, and AMOXICILLIN and CLAVULANATE potassium for oral suspension, for oral use Initial U.S. Approval: 1984 |
| 53002-7891-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-a18f-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use amoxicillin and clavulanate potassium safely and effectively. See full prescribing information for AMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS, and AMOXICILLIN AND CLAVULANATE POTASSIUM FOR ORAL SUSPENSION. AMOXICILLIN and CLAVULANATE potassium tablets, and AMOXICILLIN and CLAVULANATE potassium for oral suspension, for oral use Initial U.S. Approval: 1984 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53002-7891-2 | Amoxicillin and Clavulanate Potassium | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-7891 | AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED [RPK PHARMACEUTICALS, INC.] | 7 | Legacy NDC, 1 package rows | 20230609_9d07a3eb-e7b7-40da-8849-4650566aa785.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-7891-2 | 53002789102 | 20 TABLET, FILM COATED in 1 BOTTLE (53002-7891-2) | 2017-10-01 | 0000-00-00 | No | No | Current |