Amoxicillin and Clavulanate Potassium
- Product NDC
- 50090-3293
- 11-digit product format
- 500903293
- Labeler code
- 50090
- Product ID
- 50090-3293_b64230cb-8f9b-4ff6-9f95-639c45135e45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065162
- Marketing category
- ANDA
- Marketing start
- 2004-09-23
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 600 mg/5mL; mg/5mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3293-0 | 50090329300 | 125 mL in 1 BOTTLE (50090-3293-0) | 125 ml | 2017-12-01 | 0000-00-00 | No | No | Current |