Amoxicillin
- Product NDC
- 63187-880
- 11-digit product format
- 631870880
- Labeler code
- 63187
- Product ID
- 63187-880_31883dd0-bd99-4cde-9ded-a4c2fc3be8cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065387
- Marketing category
- ANDA
- Marketing start
- 2007-03-26
- Substance
- AMOXICILLIN
- Active strength
- 250 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 | 250 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 804826J2HU |
| Rxcui | 239191 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63187-880-15 | Amoxicillin | 150 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 150 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-880 | AMOXICILLIN POWDER, FOR SUSPENSION [PROFICIENT RX LP] | 5 | Current NDC, Legacy NDC, 1 package rows | 20220728_7f75de78-2228-48e0-8405-bf631ca431ab.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 |
|---|
| 63187-880-15 | 63187088015 | 150 mL in 1 BOTTLE (63187-880-15) | 150 ml | 2017-08-01 | 0000-00-00 | No | No | Current |