Nitrofurantoin
- Product NDC
- 0591-3684
- 11-digit product format
- 005913684
- Labeler code
- 0591
- Product ID
- 0591-3684_203cbe0b-de02-402f-8aeb-1adb0b816866
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA091095
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 25 mg/1
- Pharmacologic classes
- Nitrofuran Antibacterial [EPC], Nitrofurans [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-3684-01 | 00591368401 | 100 CAPSULE in 1 BOTTLE (0591-3684-01) | 100 capsule | 2015-10-01 | 0000-00-00 | No | No | Current |
| 0591-3684-10 | 00591368410 | 1000 CAPSULE in 1 BOTTLE (0591-3684-10) | 1000 capsule | 2015-10-01 | 0000-00-00 | No | No | Current |
| 0591-3684-30 | 00591368430 | 30 CAPSULE in 1 BOTTLE (0591-3684-30) | 30 capsule | 2015-10-01 | 0000-00-00 | No | No | Current |