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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-177-00 | Amoxicillin | 100 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-177 | AMOXICILLIN POWDER, FOR SUSPENSION [PROFICIENT RX LP] | 2 | Current NDC, Legacy NDC, 1 package rows | 20191015_45a872b8-07b1-44fe-8b57-cc572d480e2e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-177-00 | 71205017700 | 100 mL in 1 BOTTLE (71205-177-00) | 100 ml | 2018-12-01 | 0000-00-00 | No | No | Current |