Amoxicillin
- Product NDC
- 50090-6355
- 11-digit product format
- 500906355
- Labeler code
- 50090
- Product ID
- 50090-6355_ed1f5615-4881-415d-82c8-003418ade79b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065334
- Marketing category
- ANDA
- Marketing start
- 2006-12-28
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amoxicillin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMOXICILLIN | 400 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 804826J2HU |
| Rxcui | 308189 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6355-0 | Amoxicillin | 75 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 75 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6355 | AMOXICILLIN POWDER, FOR SUSPENSION [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, 1 package rows | 20240501_1dc5cc5a-59ba-4bc9-b581-cb7b70ce2652.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6355-0 | 50090635500 | 75 mL in 1 BOTTLE (50090-6355-0) | 75 ml | 2023-02-02 | No | No | Current |