Amoxicillin
- Product NDC
- 63187-200
- 11-digit product format
- 631870200
- Labeler code
- 63187
- Product ID
- 63187-200_21a6e3d2-041b-489e-9c24-8482e77ac51a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA061931
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 125 mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 804826J2HU | AMOXICILLIN | 61336-70-7 | AMOXICILLIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-200-00 | 63187020000 | 100 mL in 1 BOTTLE (63187-200-00) | 100 ml | 2014-06-02 | 0000-00-00 | No | No | Current |
| 63187-200-15 | 63187020015 | 150 mL in 1 BOTTLE (63187-200-15) | 150 ml | 2017-09-01 | 0000-00-00 | No | No | Current |
| 63187-200-80 | 63187020080 | 80 mL in 1 BOTTLE (63187-200-80) | 80 ml | 2014-06-02 | 0000-00-00 | No | No | Current |