Cephalexin
- Product NDC
- 50090-0219
- 11-digit product format
- 500900219
- Labeler code
- 50090
- Product ID
- 50090-0219_da7b8864-93bd-40e9-8607-6a9f739b8b52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA062703
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0219 | CEPHALEXIN POWDER, FOR SUSPENSION [A-S MEDICATION SOLUTIONS] | 17 | Legacy NDC | 20230306_f5f52269-9929-43bc-813e-6e45d2d5730f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0219-0 | 50090021900 | 100 mL in 1 BOTTLE (50090-0219-0) | 100 ml | 2016-06-21 | 0000-00-00 | No | No | Current |