Amoxicillan
- Product NDC
- 51655-157
- 11-digit product format
- 516550157
- Labeler code
- 51655
- Product ID
- 51655-157_7a891dd1-ed56-4f00-89fb-2d6be99252c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillan
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA062881
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#