Amoxicillin
- Product NDC
- 55289-707
- 11-digit product format
- 552890707
- Labeler code
- 55289
- Product ID
- 55289-707_7bbf8983-6d11-4c0a-e053-2a91aa0a9876
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, In
- 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-clas
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record