Amoxicillin and Clavulanate Potassium
- Product NDC
- 68071-4056
- 11-digit product format
- 680714056
- Labeler code
- 68071
- Product ID
- 68071-4056_bb2bf1f1-be82-f4cf-e053-2995a90afd0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065101
- Marketing category
- ANDA
- Marketing start
- 2002-10-31
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 68071-4056-2 | 68071405602 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-4056-2) | 2017-08-17 | 0000-00-00 | No | No | Current |