Amoxicillin
- Product NDC
- 76420-138
- 11-digit product format
- 764200138
- Labeler code
- 76420
- Product ID
- 76420-138_d964632f-4590-9500-e053-2995a90a992d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Asclemed USA, 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 |
|---|
| 76420-138-20 | Amoxicillin | 20 in 1 BOTTLE | TABLET, COATED | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-138 | AMOXICILLIN TABLET, COATED [ASCLEMED USA, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220305_23b7a1fe-4e23-44ec-bc51-5209427c88ce.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 |
|---|
| 76420-138-20 | 76420013820 | 20 TABLET, COATED in 1 BOTTLE (76420-138-20) | 2022-03-04 | 0000-00-00 | No | No | Current |