Amoxicillin
- Product NDC
- 76420-192
- 11-digit product format
- 764200192
- Labeler code
- 76420
- Product ID
- 76420-192_d19616e7-f7df-d290-e053-2995a90ae266
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA064076
- Marketing category
- ANDA
- Marketing start
- 1994-09-30
- 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 |
|---|
| 76420-192-21 | 76420019221 | 21 CAPSULE in 1 BOTTLE (76420-192-21) | 21 capsule | 2021-11-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2021-11-24 | HUMAN PRESCRIPTION DRUG LABEL | 1 |