Nystatin
- Product NDC
- 71205-106
- 11-digit product format
- 712050106
- Labeler code
- 71205
- Product ID
- 71205-106_8924a6e9-0d20-4f52-b6e7-b6683ee9eb92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nystatin
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065175
- Marketing category
- ANDA
- Marketing start
- 2014-09-01
- Marketing end
- 0000-00-00
- Substance
- NYSTATIN
- Active strength
- 100000 [USP'U]/g
- Pharmacologic classes
- Polyene Antifungal [EPC],Polyenes [CS]
- 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 |
|---|
| 71205-106 | NYSTATIN POWDER [PROFICIENT RX LP] | 3 | Legacy NDC | 20191029_2452871a-2e35-424f-afcc-7bbdf0df7b45.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-106-30 | 71205010630 | 30 g in 1 BOTTLE, PLASTIC (71205-106-30) | 30 g | 2018-09-04 | 0000-00-00 | No | No | Current |