Cefixime
- Product NDC
- 43598-673
- 11-digit product format
- 435980673
- Labeler code
- 43598
- Product ID
- 43598-673_f1643ee6-0df8-54d4-e053-2a95a90a444f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefixime
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Dr. Reddy
- Application
- ANDA206938
- Marketing category
- ANDA
- Marketing start
- 2017-08-03
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43598-673 | CEFIXIME POWDER, FOR SUSPENSION [DR. REDDY’S LABORATORIES, INC] | 10 | Legacy NDC | 20231006_f5397168-0550-4ab6-8a6d-76ada66c245b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43598-673-50 | 43598067350 | 50 mL in 1 BOTTLE (43598-673-50) | 50 ml | 2017-08-03 | 0000-00-00 | No | No | Current |