Amoxicillin and Clavulanate Potassium
- Product NDC
- 55700-653
- 11-digit product format
- 557000653
- Labeler code
- 55700
- Product ID
- 55700-653_5fc90565-f545-48dc-af79-39c847f80700
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA203824
- Marketing category
- ANDA
- Marketing start
- 2018-07-13
- Marketing end
- 2021-10-31
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875 mg/1; mg/1
- Pharmacologic classes
- beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA],Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 55700-653-20 | 55700065320 | 20 TABLET in 1 BOTTLE (55700-653-20) | 20 tablet | 2018-07-13 | 0000-00-00 | No | No | Current |