Cefaclor
- Product NDC
- 23594-125
- 11-digit product format
- 235940125
- Labeler code
- 23594
- Product ID
- 23594-125_ed37ca15-9a37-73c4-e053-2995a90a34f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefaclor
- Dosage form
- FOR SUSPENSION
- Route
- ORAL
- Labeler
- Aytu Therapeutics, LLC
- Application
- ANDA065412
- Marketing category
- ANDA
- Marketing start
- 2015-10-26
- Marketing end
- 0000-00-00
- Substance
- CEFACLOR
- Active strength
- 125 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23594-125-01 | 23594012501 | 150 mL in 1 BOTTLE, PLASTIC (23594-125-01) | 150 ml | 2015-10-26 | 0000-00-00 | No | No | Current |