NITROFURANTOIN
- Product NDC
- 70408-239
- 11-digit product format
- 704080239
- Labeler code
- 70408
- Product ID
- 70408-239_686f8b08-4e54-4cb2-abdd-595c3fb3d16e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NITROFURANTOIN
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Nostrum Laboratories, Inc.
- Application
- ANDA201355
- Marketing category
- ANDA
- Marketing start
- 2012-03-04
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 25 mg/5mL
- Pharmacologic classes
- Nitrofuran Antibacterial [EPC], Nitrofurans [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70408-239-32 | NITROFURANTOIN | 240 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 240 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70408-239 | NITROFURANTOIN SUSPENSION [NOSTRUM LABORATORIES, INC.] | 5 | Legacy NDC, 1 package rows | 20221109_c4fc70b5-f6eb-417e-8cc9-5b6e8a6e649f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70408-239-32 | 70408023932 | 240 mL in 1 BOTTLE, PLASTIC (70408-239-32) | 240 ml | 2012-03-04 | 0000-00-00 | No | No | Current |