Amoxicillin
- Product NDC
- 68788-8977
- 11-digit product format
- 687888977
- Labeler code
- 68788
- Product ID
- 68788-8977_85308e96-d3bc-47fd-b9b7-3988db75e605
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065256
- Marketing category
- ANDA
- Marketing start
- 2016-01-20
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#