Cephalexin
- Product NDC
- 66267-981
- 11-digit product format
- 662670981
- Labeler code
- 66267
- Product ID
- 66267-981_9cadb284-f2ee-9079-e053-2a95a90a2d82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065326
- Marketing category
- ANDA
- Marketing start
- 2007-04-12
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66267-981-20 | Cephalexin | 200 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 200 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66267-981 | CEPHALEXIN POWDER, FOR SUSPENSION [NUCARE PHARMACEUTICALS,INC.] | 3 | Legacy NDC, 1 package rows | 20200401_5c60a424-8ec5-003e-e053-2a91aa0ab3f0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 66267-981-20 | 66267098120 | 200 mL in 1 BOTTLE | 200 ml | Historical |