Amoxicillin
- Product NDC
- 68071-5019
- 11-digit product format
- 680715019
- Labeler code
- 68071
- Product ID
- 68071-5019_1ceb908d-da9a-515a-e063-6394a90ad07c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065271
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-5019-4 | 68071501904 | 4 CAPSULE in 1 BOTTLE (68071-5019-4) | 4 capsule | 2019-08-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | NuCare Pharmaceuticals,Inc. | 2024-07-10 | HUMAN PRESCRIPTION DRUG LABEL | 5 |