Nitrofurantoin
- Product NDC
- 68071-2281
- 11-digit product format
- 680712281
- Labeler code
- 68071
- Product ID
- 68071-2281_d7759453-1a75-8fd9-e053-2a95a90ad895
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA091095
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Nitrofuran Antibacterial [EPC], Nitrofurans [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 |
|---|
| 68071-2281-2 | 68071228102 | 2 CAPSULE in 1 BOTTLE (68071-2281-2) | 2 capsule | 2020-10-22 | 0000-00-00 | No | No | Current |