Amoxicillin
- Product NDC
- 72789-224
- 11-digit product format
- 727890224
- Labeler code
- 72789
- Product ID
- 72789-224_40ad11b9-8246-8d3f-e063-6294a90a26eb
- 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 |
|---|
| 72789-224-01 | Amoxicillin | 100 in 1 BOTTLE, PLASTIC | TABLET, COATED | 100 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-224 | AMOXICILLIN TABLET, COATED [PD-RX PHARMACEUTICALS, INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20241001_b397d4be-d2ef-419a-98ac-844069c99d56.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 |
|---|
| 72789-224-01 | 72789022401 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (72789-224-01) | 2022-02-10 | 0000-00-00 | No | No | Current |