Amoxicillin
- Product NDC
- 63629-5730
- 11-digit product format
- 636295730
- Labeler code
- 63629
- Product ID
- 63629-5730_2dbe0ab6-f36b-4c21-82c1-ec72d1b6687d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065271
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- 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 |
|---|
| 63629-5730-1 | 63629573001 | 15 CAPSULE in 1 BOTTLE (63629-5730-1) | 15 capsule | 2025-06-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | Bryant Ranch Prepack | 2025-06-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |