Amoxicillin
- Product NDC
- 43063-885
- 11-digit product format
- 430630885
- Labeler code
- 43063
- Product ID
- 43063-885_2cf156b1-81d6-05eb-e063-6394a90aa475
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA065255
- Marketing category
- ANDA
- Marketing start
- 2006-03-29
- Substance
- AMOXICILLIN
- Active strength
- 875 mg/1
- 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 | 875 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 804826J2HU |
| Rxcui | 308194 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43063-885-20 | Amoxicillin | 20 in 1 BOTTLE, PLASTIC | TABLET, COATED | 20 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-885 | AMOXICILLIN TABLET, COATED [PD-RX PHARMACEUTICALS, INC.] | 13 | Current NDC, Legacy NDC, 1 package rows | 20250131_05b9b595-05d9-469f-82a3-c2bc94c50be2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-885-20 | 43063088520 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-885-20) | 2018-08-16 | 0000-00-00 | No | No | Current |