NDC 69621-821

Zeyocaine

Lidocaine, Isopropyl Alcohol

Zeyocaine is a Topical Kit in the Human Prescription Drug category. It is labeled and distributed by Shoreline Pharmaceuticals, Inc.. The primary component is .

• Product ID: 69621-821_dfa240db-ef4b-4d10-8196-ac578e47ce15
• NDC: 69621-821
• Product Type: Human Prescription Drug
• Proprietary Name: Zeyocaine
• Generic Name: Lidocaine, Isopropyl Alcohol
• Dosage Form: Kit
• Route of Administration: TOPICAL
• Marketing Start Date: 2016-09-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA205318
• Labeler Name: Shoreline Pharmaceuticals, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 69621-821-00

1 KIT in 1 CARTON (69621-821-00) * 30 in 1 CARTON * 200 POUCH in 1 PACKAGE (67777-121-13) > .55 mL in 1 POUCH * 1 TUBE in 1 CARTON (52565-008-14) > 35.44 g in 1 TUBE

• Marketing Start Date: 2016-09-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69621-821-00 [69621082100]

Zeyocaine KIT

• Marketing Category: ANDA
• Application Number: ANDA205318
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-09-30
• Marketing End Date: 2019-05-15

Drug Details

OpenFDA Data

• SPL SET ID: 135c324b-0c9a-48a3-be0a-c7e7c5f4de20
• Manufacturer:
  • Shoreline Pharmaceuticals, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 797544
  • 1543069

NDC Crossover Matching brand name "Zeyocaine" or generic name "Lidocaine, Isopropyl Alcohol"

NDC	Brand Name	Generic Name
69621-821	Zeyocaine	lidocaine, isopropyl alcohol
80672-003	Super Magic Man Premium Gold	Lidocaine, Isopropyl Alcohol