Amoxicillin and Clavulanate Potassium
- Product NDC
- 68071-3107
- 11-digit product format
- 680713107
- Labeler code
- 68071
- Product ID
- 68071-3107_d5cbb013-7d90-27b4-e053-2995a90a4474
- 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
- 2023-12-31
- 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 |
|---|
| 68071-3107-3 | 68071310703 | 3 TABLET, FILM COATED in 1 BOTTLE (68071-3107-3) | 2017-03-14 | 0000-00-00 | No | No | Current |
| 68071-3107-4 | 68071310704 | 4 TABLET, FILM COATED in 1 BOTTLE (68071-3107-4) | 2017-03-14 | 0000-00-00 | No | No | Current |