Amoxicillin and Clavulanate Potassium
- Product NDC
- 35356-982
- 11-digit product format
- 353560982
- Labeler code
- 35356
- Product ID
- 35356-982_bb9e2482-8e19-410a-806b-e867670c7a39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
- Application
- ANDA091569
- Marketing category
- ANDA
- Marketing start
- 2012-01-20
- Marketing end
- 2021-10-31
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 500 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35356-982-20 | 35356098220 | 20 TABLET, FILM COATED in 1 BOTTLE (35356-982-20) | 2012-01-20 | 2021-10-31 | No | No | Current |