NDC 59088-391

DermacinRx Clorhexacin

Mupirocin Ointment

DermacinRx Clorhexacin is a Kit in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is .

• Product ID: 59088-391_4921fe39-f86c-4723-98d2-cde68dbae88a
• NDC: 59088-391
• Product Type: Human Prescription Drug
• Proprietary Name: DermacinRx Clorhexacin
• Generic Name: Mupirocin Ointment
• Dosage Form: Kit
• Marketing Start Date: 2016-06-02
• Marketing Category: ANDA / ANDA
• Application Number: ANDA065123
• Labeler Name: PureTek Corporation
• Active Ingredient Strength: 0
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 59088-391-00

1 KIT in 1 CARTON (59088-391-00) * 237 mL in 1 BOTTLE, PLASTIC (0116-1061-08) * 118 mL in 1 TUBE (59088-333-08) * 1 TUBE in 1 CARTON (45802-112-22) > 22 g in 1 TUBE

• Marketing Start Date: 2016-06-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59088-391-00 [59088039100]

DermacinRx Clorhexacin KIT

• Marketing Category: ANDA
• Application Number: ANDA065123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-06-02

Drug Details

OpenFDA Data

• SPL SET ID: 3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f9
• Manufacturer:
  • PureTek Corporation
• RxNorm Concept Unique ID - RxCUI:
  • 106346
  • 211365
  • 259090