Nitrofurantoin
- Product NDC
- 68071-5050
- 11-digit product format
- 680715050
- Labeler code
- 68071
- Product ID
- 68071-5050_bbb3f437-cdec-3abc-e053-2995a90a44b1
- 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
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-5050-7 | 68071505007 | 14 CAPSULE in 1 BOTTLE (68071-5050-7) | 14 capsule | 2019-09-05 | 0000-00-00 | No | No | Current |