Cephalexin
- Product NDC
- 55700-620
- 11-digit product format
- 557000620
- Labeler code
- 55700
- Product ID
- 55700-620_e697652a-9c25-48c2-97a1-8ba6d3b1ddc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090836
- Marketing category
- ANDA
- Marketing start
- 2018-05-18
- Marketing end
- 2021-10-31
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| OBN7UDS42Y | CEPHALEXIN | 23325-78-2 | CEPHALEXIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-620-30 | 55700062030 | 30 CAPSULE in 1 BOTTLE (55700-620-30) | 30 capsule | 2018-05-18 | 2021-10-31 | No | No | Current |