AMOXICILLIN AND CLAVULANATE POTASSIUM
- Product NDC
- 68071-3402
- 11-digit product format
- 680713402
- Labeler code
- 68071
- Product ID
- 68071-3402_0f3c200e-eb4c-5c2d-e063-6294a90a8342
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204755
- Marketing category
- ANDA
- Marketing start
- 2017-03-01
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875; 125 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AMOXICILLIN AND CLAVULANATE POTASSIUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMOXICILLIN | 875 mg/1 |
| CLAVULANATE POTASSIUM | 125 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 804826J2HU, Q42OMW3AT8 |
| Rxcui | 562508 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3402-1 | AMOXICILLIN AND CLAVULANATE POTASSIUM | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 4 |
| 68071-3402-3 | AMOXICILLIN AND CLAVULANATE POTASSIUM | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
| 68071-3402-4 | AMOXICILLIN AND CLAVULANATE POTASSIUM | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 4 |
| 68071-3402-8 | AMOXICILLIN AND CLAVULANATE POTASSIUM | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3402 | AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 4 | Current NDC, 4 package rows | 20240119_fbd40fcd-bf5b-e91e-e053-6394a90a609c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3402-1 | 68071340201 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-3402-1) | 2023-06-21 | No | No | Current |
| 68071-3402-3 | 68071340203 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3402-3) | 2023-05-16 | No | No | Current |
| 68071-3402-4 | 68071340204 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-3402-4) | 2023-05-16 | No | No | Current |
| 68071-3402-8 | 68071340208 | 28 TABLET, FILM COATED in 1 BOTTLE (68071-3402-8) | 2023-06-21 | No | No | Current |