Cefaclor
- Product NDC
- 63629-1007
- 11-digit product format
- 636291007
- Labeler code
- 63629
- Product ID
- 63629-1007_42d6e553-875b-4c77-a161-3bb02c1f23b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefaclor
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065146
- Marketing category
- ANDA
- Marketing start
- 2008-07-31
- 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
- 2023-12-31
- 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 |
|---|
| 63629-1007-3 | 63629100703 | 30 CAPSULE in 1 BOTTLE (63629-1007-3) | 30 capsule | 2022-04-14 | 0000-00-00 | No | No | Current |