AMOXIL
- Product NDC
- 61919-135
- 11-digit product format
- 619190135
- Labeler code
- 61919
- Product ID
- 61919-135_f2026976-ae4b-a6ea-e053-2a95a90ae6ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMOXICILLIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065256
- Marketing category
- ANDA
- Marketing start
- 2016-07-08
- 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
- 2024-12-31
- 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 |
|---|
| 61919-135-20 | AMOXIL | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-135 | AMOXIL (AMOXICILLIN) TABLET, FILM COATED [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20230112_375cdfd0-7996-5a42-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 |
|---|
| 61919-135-20 | 61919013520 | 20 TABLET, FILM COATED in 1 BOTTLE (61919-135-20) | 2016-07-08 | 0000-00-00 | No | No | Current |