Amoxicillin
- Product NDC
- 42708-011
- 11-digit product format
- 427080011
- Labeler code
- 42708
- Product ID
- 42708-011_3a2ba488-2d7a-4288-b49c-088777faed98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA065255
- Marketing category
- ANDA
- Marketing start
- 2006-03-29
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#