Amoxicillin
- Product NDC
- 63187-195
- 11-digit product format
- 631870195
- Labeler code
- 63187
- Product ID
- 63187-195_c35169e7-1e15-4748-98a2-38fff0a10323
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065322
- Marketing category
- ANDA
- Marketing start
- 2006-06-19
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 600 mg/5mL; mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63187-195-12 | 63187019512 | 125 mL in 1 BOTTLE (63187-195-12) | 125 ml | 2014-05-01 | 0000-00-00 | No | No | Current |