Amoxicillin
- Product NDC
- 63187-138
- 11-digit product format
- 631870138
- Labeler code
- 63187
- Product ID
- 63187-138_a4366ae8-cae5-43b2-9403-d2b9c08b9f12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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