Amoxicillin
- Product NDC
- 50090-6355
- 11-digit product format
- 500906355
- Labeler code
- 50090
- Product ID
- 50090-6355_ed1f5615-4881-415d-82c8-003418ade79b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065334
- Marketing category
- ANDA
- Marketing start
- 2006-12-28
- Substance
- AMOXICILLIN
- Active strength
- 400 mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 50090-6355-0 | 50090635500 | 75 mL in 1 BOTTLE (50090-6355-0) | 75 ml | 2023-02-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | A-S Medication Solutions | 2024-04-30 | Human Prescription Drug Label | 3 |