Amoxicillin and Clavulanate Potassium
- Product NDC
- 68788-7805
- 11-digit product format
- 687887805
- Labeler code
- 68788
- Product ID
- 68788-7805_dfaeacf7-91e4-4b37-a465-3bfd1142638f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203824
- Marketing category
- ANDA
- Marketing start
- 2020-10-28
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7805-2 | 68788780502 | 20 TABLET in 1 BOTTLE (68788-7805-2) | 20 tablet | 2020-10-28 | 0000-00-00 | No | No | Current |