Amoxicillin
- Product NDC
- 71205-422
- 11-digit product format
- 712050422
- Labeler code
- 71205
- Product ID
- 71205-422_ffdf60e8-a414-4675-8e7d-8e90ebab3614
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065325
- Marketing category
- ANDA
- Marketing start
- 2006-06-19
- Substance
- AMOXICILLIN
- Active strength
- 400 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 |
|---|
| 71205-422-00 | 71205042200 | 100 mL in 1 BOTTLE (71205-422-00) | 100 ml | 2020-03-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | Proficient Rx LP | 2022-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |