Nitrofurantoin
- Product NDC
- 70934-129
- 11-digit product format
- 709340129
- Labeler code
- 70934
- Product ID
- 70934-129_b980500b-2b8f-2024-e053-2995a90ae16a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin monohydrate/macrocrystals
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA207372
- Marketing category
- ANDA
- Marketing start
- 2018-05-25
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN MONOHYDRATE; NITROFURANTOIN
- Active strength
- 75 mg/1; mg/1
- Pharmacologic classes
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC],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 |
|---|
| 70934-129-14 | 70934012914 | 14 CAPSULE in 1 BOTTLE, PLASTIC (70934-129-14) | 14 capsule | 2018-05-25 | 0000-00-00 | No | No | Current |