Amoxicillin
- Product NDC
- 50090-0454
- 11-digit product format
- 500900454
- Labeler code
- 50090
- Product ID
- 50090-0454_f0d75b11-8892-4885-a77d-4a57d0c69246
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA064013
- Marketing category
- ANDA
- Marketing start
- 1993-01-01
- Substance
- AMOXICILLIN
- Active strength
- 250 mg/1
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-0454-0 | 50090045400 | 30 TABLET, CHEWABLE in 1 BOTTLE (50090-0454-0) | 2016-06-29 | No | No | Historical |
| 50090-0454-1 | 50090045401 | 21 TABLET, CHEWABLE in 1 BOTTLE (50090-0454-1) | 2016-06-29 | No | No | Historical |
| 50090-0454-5 | 50090045405 | 40 TABLET, CHEWABLE in 1 BOTTLE (50090-0454-5) | 2016-06-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | A-S Medication Solutions | 2024-02-13 | HUMAN PRESCRIPTION DRUG LABEL | 19 |