AMOXICILLIN AND CLAVULANATE POTASSIUM
- Product NDC
- 72162-2433
- 11-digit product format
- 721622433
- Labeler code
- 72162
- Product ID
- 72162-2433_1fa0ff58-3b58-4542-8d1a-ba016ddfd489
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205707
- Marketing category
- ANDA
- Marketing start
- 2017-03-01
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 500; 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 804826J2HU | AMOXICILLIN | 61336-70-7 | AMOXICILLIN |
| Q42OMW3AT8 | CLAVULANATE POTASSIUM | 61177-45-5 | CLAVULANATE POTASSIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2433-1 | 72162243301 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2433-1) | 2024-12-16 | No | No | Historical |
| 72162-2433-2 | 72162243302 | 20 TABLET, FILM COATED in 1 BOTTLE (72162-2433-2) | 2024-12-16 | No | No | Historical |