CEFACLOR
- Product NDC
- 0143-9985
- 11-digit product format
- 001439985
- Labeler code
- 0143
- Product ID
- 0143-9985_79869725-288c-4691-a0d3-8d02b7caf510
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFACLOR
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA065350
- Marketing category
- ANDA
- Marketing start
- 2007-05-01
- Marketing end
- 0000-00-00
- Substance
- CEFACLOR
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-9985-01 | 00143998501 | 100 CAPSULE in 1 BOTTLE (0143-9985-01) | 100 capsule | 2007-05-01 | 0000-00-00 | No | No | Current |
| 0143-9985-15 | 00143998515 | 15 CAPSULE in 1 BOTTLE (0143-9985-15) | 15 capsule | 2007-05-01 | 0000-00-00 | No | No | Current |