NDC 72275-705

Zenevix

Lidocaine Patch, Sublingual Tincture

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

• Product ID: 72275-705_85174497-dddc-ae3d-e053-2991aa0adf3b
• NDC: 72275-705
• Product Type: Human Prescription Drug
• Proprietary Name: Zenevix
• Generic Name: Lidocaine Patch, Sublingual Tincture
• Dosage Form: Kit
• Marketing Start Date: 2019-03-17
• Marketing Category: ANDA / ANDA
• Application Number: ANDA200675
• Labeler Name: Primary Pharmaceuticals, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72275-705-77

1 BOTTLE, DROPPER in 1 CARTON (72275-705-77) > 1 PATCH in 1 BOTTLE, DROPPER > 1 KIT in 1 PATCH * 30 POUCH in 1 CARTON (0591-3525-30) > 1 g in 1 POUCH * 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2019-03-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72275-705-77 [72275070577]

Zenevix KIT

• Marketing Category: ANDA
• Application Number: ANDA200675
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-03-17

Drug Details

OpenFDA Data

• SPL SET ID: 85174497-dddb-ae3d-e053-2991aa0adf3b
• Manufacturer:
  • Primary Pharmaceuticals, Inc.