Nitrofurantoin
- Product NDC
- 71205-365
- 11-digit product format
- 712050365
- Labeler code
- 71205
- Product ID
- 71205-365_faf559f7-a748-4501-8cfb-8924122441f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091095
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 50 mg/1
- Pharmacologic classes
- 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 |
|---|
| 71205-365 | NITROFURANTOIN CAPSULE [PROFICIENT RX LP] | 1 | Legacy NDC | 20191128_faf559f7-a748-4501-8cfb-8924122441f3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-365-14 | 71205036514 | 14 CAPSULE in 1 BOTTLE (71205-365-14) | 14 capsule | 2019-11-01 | 0000-00-00 | No | No | Current |