Cephalexin
- Product NDC
- 51655-125
- 11-digit product format
- 516550125
- Labeler code
- 51655
- Product ID
- 51655-125_4afc9b83-70f5-4d70-a7e2-6fb333dd7ae6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA065229
- Marketing category
- ANDA
- Marketing start
- 2014-06-20
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-125 | CEPHALEXIN CAPSULE [NORTHWIND PHARMACEUTICALS] | 3 | Legacy NDC | 20141001_694e406b-0dbd-47ef-b176-64d78ca836fa.zip |