Amoxicillin
- Product NDC
- 71205-177
- 11-digit product format
- 712050177
- Labeler code
- 71205
- Product ID
- 71205-177_aefe01bd-575f-4718-872e-b5d89f4916b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065119
- Marketing category
- ANDA
- Marketing start
- 2003-02-26
- 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 |
|---|
| 71205-177-00 | 71205017700 | 100 mL in 1 BOTTLE (71205-177-00) | 100 ml | 2018-12-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | Proficient Rx LP | 2019-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |