Amoxicillin
- Product NDC
- 50090-4325
- 11-digit product format
- 500904325
- Labeler code
- 50090
- Product ID
- 50090-4325_43ed2640-1a4d-4363-8568-cd2c1cb499d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA061926
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-4325-0 | 50090432500 | 30 CAPSULE in 1 BOTTLE (50090-4325-0) | 30 capsule | 2019-05-30 | 0000-00-00 | No | No | Current |
| 50090-4325-1 | 50090432501 | 30 CAPSULE in 1 BOTTLE (50090-4325-1) | 30 capsule | 2019-05-30 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | A-S Medication Solutions | 2020-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 4 |