Amoxicillin
- Product NDC
- 68071-2558
- 11-digit product format
- 680712558
- Labeler code
- 68071
- Product ID
- 68071-2558_2dcc5889-6ad9-d3dc-e063-6294a90a50f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA061931
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Substance
- AMOXICILLIN
- Active strength
- 250 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 |
|---|
| 68071-2558-5 | 68071255805 | 150 mL in 1 BOTTLE (68071-2558-5) | 150 ml | 2021-10-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | NuCare Pharmaceuticals,Inc. | 2025-02-10 | HUMAN PRESCRIPTION DRUG LABEL | 3 |