AMOXICILLIN AND CLAVULANATE POTASSIUM
- Product NDC
- 51655-160
- 11-digit product format
- 516550160
- Labeler code
- 51655
- Product ID
- 51655-160_d8c1bbab-8384-4098-92f5-d3446aa8f541
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMOXICILLIN AND CLAVULANATE POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals. LLC
- Application
- ANDA065096
- Marketing category
- ANDA
- Marketing start
- 2014-07-18
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875 mg/1; mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-160 | AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS. LLC] | 1 | Legacy NDC | 20140731_61eaa530-43e1-4964-81ff-8e9ffaa7521c.zip |