Nitrofurantoin
- Product NDC
- 68001-423
- 11-digit product format
- 680010423
- Labeler code
- 68001
- Product ID
- 68001-423_559f763c-db04-47b2-90ff-d820b2070c3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA208516
- Marketing category
- ANDA
- Marketing start
- 2019-11-13
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC],Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-423 | NITROFURANTOIN CAPSULE [BLUEPOINT LABORATORIES] | 2 | Legacy NDC | 20250322_559f763c-db04-47b2-90ff-d820b2070c3c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-423-00 | 68001042300 | 100 CAPSULE in 1 BOTTLE (68001-423-00) | 100 capsule | 2019-11-13 | 0000-00-00 | No | No | Current |