Cephalexin
- Product NDC
- 15749-802
- 11-digit product format
- 157490802
- Labeler code
- 15749
- Product ID
- 15749-802_da2a32ef-7ed4-4a3f-8e0d-326c91b191c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Antibiotics, Inc
- Application
- ANDA062713
- Marketing category
- ANDA
- Marketing start
- 2011-06-15
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 15749-802-02 | Cephalexin | 100 in 1 BOTTLE | CAPSULE | 100 | | 1 |
| 15749-802-08 | Cephalexin | 500 in 1 BOTTLE | CAPSULE | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 15749-802 | CEPHALEXIN CAPSULE [AMERICAN ANTIBIOTICS, INC] | 1 | Legacy NDC, 2 package rows | 20110621_5de0f7c1-d152-45f7-bfb7-9e5404d9f74b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 15749-802-02 | 15749080202 | 100 in 1 BOTTLE | Historical |
| 15749-802-08 | 15749080208 | 500 in 1 BOTTLE | Historical |