Amoxicillin
- Product NDC
- 66267-549
- 11-digit product format
- 662670549
- Labeler code
- 66267
- Product ID
- 66267-549_9cbeac96-5345-3898-e053-2995a90aae67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA065256
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record