AMOXIL
- Product NDC
- 61919-041
- 11-digit product format
- 619190041
- Labeler code
- 61919
- Product ID
- 61919-041_9c590d56-67e9-bfdd-e053-2995a90a02f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMOXICILLIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065255
- Marketing category
- ANDA
- Marketing start
- 2015-06-05
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 875 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 |
|---|
| 61919-041-20 | AMOXIL | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-041 | AMOXIL (AMOXICILLIN) TABLET, FILM COATED [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200129_3388e873-132a-346b-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-041-20 | 61919004120 | 20 TABLET, FILM COATED in 1 BOTTLE (61919-041-20) | 2015-06-05 | 0000-00-00 | No | No | Current |