Nystatin
- Product NDC
- 39822-3015
- 11-digit product format
- 398223015
- Labeler code
- 39822
- Product ID
- 39822-3015_eedc4d46-9206-09f1-e053-2995a90aecf6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nystatin
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Application
- ANDA065175
- Marketing category
- ANDA
- Marketing start
- 2004-08-30
- 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
- 2023-12-31
- 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 |
|---|
| 39822-3015-1 | 39822301501 | 15 g in 1 BOTTLE, PLASTIC (39822-3015-1) | 15 g | 2004-08-30 | 0000-00-00 | No | No | Current |
| 39822-3015-3 | 39822301503 | 30 g in 1 BOTTLE, PLASTIC (39822-3015-3) | 30 g | 2004-08-30 | 0000-00-00 | No | No | Current |
| 39822-3015-6 | 39822301506 | 60 g in 1 BOTTLE, PLASTIC (39822-3015-6) | 60 g | 2004-08-30 | 0000-00-00 | No | No | Current |