Nitrofurantoin
- Product NDC
- 50090-3856
- 11-digit product format
- 500903856
- Labeler code
- 50090
- Product ID
- 50090-3856_f3203339-9626-434c-a410-631632c777e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin (monohydrate/macrocrystals)
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077066
- Marketing category
- ANDA
- Marketing start
- 2005-04-06
- 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 |
|---|
| 50090-3856-0 | 50090385600 | 14 CAPSULE in 1 BOTTLE (50090-3856-0) | 14 capsule | 2018-11-21 | 0000-00-00 | No | No | Current |
| 50090-3856-1 | 50090385601 | 10 CAPSULE in 1 BOTTLE (50090-3856-1) | 10 capsule | 2019-11-05 | 0000-00-00 | No | No | Current |