SUPRAX
- Product NDC
- 70518-2006
- 11-digit product format
- 705182006
- Labeler code
- 70518
- Product ID
- 70518-2006_86244478-07f0-94cf-e053-2a91aa0ac94a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA203195
- Marketing category
- NDA
- Marketing start
- 2019-04-09
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 400 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record