Permethrin
- Product NDC
- 53002-9570
- 11-digit product format
- 530029570
- Labeler code
- 53002
- Product ID
- 53002-9570_4eb92998-b294-4b87-91ce-60f8c143c1f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Permethrin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA076369
- Marketing category
- ANDA
- Marketing start
- 2006-08-11
- Marketing end
- 0000-00-00
- Substance
- PERMETHRIN
- Active strength
- 50 mg/g
- Pharmacologic classes
- Pyrethrins [CS],Pyrethroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53002-9570-1 | Permethrin | 60 g in 1 TUBE | CREAM | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-9570 | PERMETHRIN CREAM [RPK PHARMACEUTICALS, INC.] | 5 | Legacy NDC, 1 package rows | 20230609_041444b6-a71e-4d13-8d24-f2d104bf721d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-9570-1 | 53002957001 | 60 g in 1 TUBE (53002-9570-1) | 60 g | 2018-10-01 | 0000-00-00 | No | No | Current |