NDC 76439-102 - CEPHALEXIN
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 76439-102
- Manufacturer
- DIRECT RX
- Effective date
- 2015-08-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CEPHALEXIN - DIRECT RX | DIRECT RX | 2015-08-10 | HUMAN PRESCRIPTION DRUG LABEL |
| CEPHALEXIN CAPSULES, USP | Blenheim Pharmacal, Inc. | 2015-04-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Cephalexin - ReadyMeds | ReadyMeds | 2014-05-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Cephalexin - TYA Pharmaceuticals | TYA Pharmaceuticals | 2012-02-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 76439-102-10 | EA - Each | 76439-102 | 7d7ddf90-ea26-4824-a5db-36d510460c98 | 1 | 2012-07-24 |
| 76439-102-50 | EA - Each | 76439-102 | 371c320d-eeb3-42d8-85db-5719383d6d0c | 1 | 2012-07-24 |