Amoxicillin and Clavulanate Potassium
- Product NDC
- 68071-2502
- 11-digit product format
- 680712502
- Labeler code
- 68071
- Product ID
- 68071-2502_e5448cb5-c0f8-6709-e053-2995a90a5ff5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065096
- Marketing category
- ANDA
- Marketing start
- 2002-10-31
- 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
- 2023-12-31
- 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 |
|---|
| 68071-2502-2 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9c94-d83d-e063-dadaa90ab31f | These highlights do not include all the information needed to use Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable) safely and effectively. See full prescribing information for Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable). AMOXICILLIN AND CLAVULANAT |
| 68071-2502-3 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9c94-d83d-e063-dadaa90ab31f | These highlights do not include all the information needed to use Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable) safely and effectively. See full prescribing information for Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable). AMOXICILLIN AND CLAVULANAT |
| 68071-2502-4 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9c94-d83d-e063-dadaa90ab31f | These highlights do not include all the information needed to use Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable) safely and effectively. See full prescribing information for Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable). AMOXICILLIN AND CLAVULANAT |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2502-2 | Amoxicillin and Clavulanate Potassium | 2 in 1 BOTTLE | TABLET, FILM COATED | 2 | | 2 |
| 68071-2502-3 | Amoxicillin and Clavulanate Potassium | 3 in 1 BOTTLE | TABLET, FILM COATED | 3 | | 2 |
| 68071-2502-4 | Amoxicillin and Clavulanate Potassium | 4 in 1 BOTTLE | TABLET, FILM COATED | 4 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2502 | AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 2 | Legacy NDC, 3 package rows | 20220804_c94f2f22-0855-eca7-e053-2a95a90a4ced.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 |
|---|
| 68071-2502-2 | 68071250202 | 2 TABLET, FILM COATED in 1 BOTTLE (68071-2502-2) | 2021-08-11 | 0000-00-00 | No | No | Current |
| 68071-2502-3 | 68071250203 | 3 TABLET, FILM COATED in 1 BOTTLE (68071-2502-3) | 2021-08-11 | 0000-00-00 | No | No | Current |
| 68071-2502-4 | 68071250204 | 4 TABLET, FILM COATED in 1 BOTTLE (68071-2502-4) | 2021-08-11 | 0000-00-00 | No | No | Current |