CEPHALEXIN ORAL SUSP
- Product NDC
- 61919-798
- 11-digit product format
- 619190798
- Labeler code
- 61919
- Product ID
- 61919-798_85a53325-1307-7e6a-e053-2991aa0a2db5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEPHALEXIN ORAL SUSP
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- ANDA065152
- Marketing category
- ANDA
- Marketing start
- 2019-04-03
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 61919-798-32 | 61919079832 | 100 mL in 1 BOTTLE (61919-798-32) | 100 ml | 2019-04-03 | 0000-00-00 | No | No | Current |