AMOXICILLIN
- Product NDC
- 61919-623
- 11-digit product format
- 619190623
- Labeler code
- 61919
- Product ID
- 61919-623_9c58dc5b-7dda-54b9-e053-2995a90ad423
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMOXICILLIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065256
- Marketing category
- ANDA
- Marketing start
- 2016-12-01
- 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 |
|---|
| 61919-623-20 | AMOXICILLIN | 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 |
|---|
| 61919-623 | AMOXICILLIN TABLET, FILM COATED [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200118_429a7c98-cb01-4059-e054-00144ff88e88.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 |
|---|
| 61919-623-20 | 61919062320 | 20 TABLET, FILM COATED in 1 BOTTLE (61919-623-20) | 2016-12-01 | 0000-00-00 | No | No | Current |