Amoxicillin
- Product NDC
- 53002-2080
- 11-digit product format
- 530022080
- Labeler code
- 53002
- Product ID
- 53002-2080_700b79b4-7c37-415a-990d-3f97fb1e9e84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA065271
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 250 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53002-2080-1 | Amoxicillin | 30 in 1 BOTTLE | CAPSULE | 30 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-2080 | AMOXICILLIN CAPSULE [RPK PHARMACEUTICALS, INC.] | 11 | Legacy NDC, 1 package rows | 20230609_23979212-e989-4a8e-8dc8-46c5b4ecd590.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 |
|---|
| 53002-2080-1 | 53002208001 | 30 CAPSULE in 1 BOTTLE (53002-2080-1) | 30 capsule | 2017-10-01 | 0000-00-00 | No | No | Current |