Nitrofurantion
- Product NDC
- 70518-3041
- 11-digit product format
- 705183041
- Labeler code
- 70518
- Product ID
- 70518-3041_bcd0d483-f508-4c7c-e053-2995a90a5733
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantion
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201722
- Marketing category
- ANDA
- Marketing start
- 2021-03-05
- 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 |
|---|
| 70518-3041-0 | 70518304100 | 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-3041-0) | 14 capsule | 2021-03-05 | 0000-00-00 | No | No | Current |