Cephalexin
- Product NDC
- 70934-082
- 11-digit product format
- 709340082
- Labeler code
- 70934
- Product ID
- 70934-082_d2447a7b-2423-84ff-e053-2995a90a4c82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065229
- Marketing category
- ANDA
- Marketing start
- 2018-03-05
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-082-20 | 70934008220 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-082-20) | 20 capsule | 2020-01-30 | 0000-00-00 | No | No | Current |
| 70934-082-30 | 70934008230 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-082-30) | 30 capsule | 2018-09-07 | 0000-00-00 | No | No | Current |
| 70934-082-94 | 70934008294 | 30 CAPSULE in 1 DOSE PACK (70934-082-94) | 30 capsule | 2018-03-05 | 0000-00-00 | No | No | Current |