Amoxicillin
- Product NDC
- 72789-225
- 11-digit product format
- 727890225
- Labeler code
- 72789
- Product ID
- 72789-225_40ad11b9-8247-8d3f-e063-6294a90a26eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA065291
- Marketing category
- ANDA
- Marketing start
- 2007-03-01
- Substance
- AMOXICILLIN
- Active strength
- 500 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-225-82 | 72789022582 | 500 CAPSULE in 1 BOTTLE, PLASTIC (72789-225-82) | 500 capsule | 2022-02-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | PD-Rx Pharmaceuticals, Inc. | 2025-10-08 | HUMAN PRESCRIPTION DRUG LABEL | 26 |
| Amoxicillin | PD-Rx Pharmaceuticals, Inc. | 2024-11-19 | HUMAN PRESCRIPTION DRUG LABEL | 25 |