Nystop
- Product NDC
- 71335-2845
- 11-digit product format
- 713352845
- Labeler code
- 71335
- Product ID
- 71335-2845_0cf86c4a-028c-48d9-88cf-937059ecd907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nystatin
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA064118
- Marketing category
- ANDA
- Marketing start
- 1996-08-16
- Substance
- NYSTATIN
- Active strength
- 100000 [USP'U]/g
- Pharmacologic classes
- Polyene Antifungal [EPC], Polyenes [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| BDF1O1C72E | NYSTATIN | 1400-61-9 | NYSTATIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2845-1 | 71335284501 | 15 g in 1 BOTTLE, PLASTIC (71335-2845-1) | 15 g | 2025-10-21 | No | No | Historical |