NDC 61388-001

Zingo

Lidocaine Hydrochloride Monohydrate

Zingo is a Intradermal Powder in the Human Prescription Drug category. It is labeled and distributed by Powder Pharmaceuticals Inc.. The primary component is Lidocaine Hydrochloride.

• Product ID: 61388-001_8a718360-be4c-4dea-b9bc-e9e4beff29b5
• NDC: 61388-001
• Product Type: Human Prescription Drug
• Proprietary Name: Zingo
• Generic Name: Lidocaine Hydrochloride Monohydrate
• Dosage Form: Powder
• Route of Administration: INTRADERMAL
• Marketing Start Date: 2015-01-05
• Marketing Category: NDA / NDA
• Application Number: NDA022114
• Labeler Name: Powder Pharmaceuticals Inc.
• Substance Name: LIDOCAINE HYDROCHLORIDE
• Active Ingredient Strength: 1 mg/1
• Pharm Classes: Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 61388-001-48

12 POUCH in 1 CARTON (61388-001-48) > 1 POWDER in 1 POUCH

• Marketing Start Date: 2015-01-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61388-001-48 [61388000148]

Zingo POWDER

• Marketing Category: NDA
• Application Number: NDA022114
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-01-05
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
LIDOCAINE HYDROCHLORIDE	.5 mg/1

OpenFDA Data

• SPL SET ID: ea5416d6-5988-413b-8682-6835b359eb78
• Manufacturer:
  • Powder Pharmaceuticals Inc.
• UNII:
  • V13007Z41A
• RxNorm Concept Unique ID - RxCUI:
  • 1011709
  • 1011707
• UPC Code:
  • 0353329200577

Pharmacological Class

• Amide Local Anesthetic [EPC]
• Amides [CS]
• Antiarrhythmic [EPC]
• Local Anesthesia [PE]

NDC Crossover Matching brand name "Zingo" or generic name "Lidocaine Hydrochloride Monohydrate"

NDC	Brand Name	Generic Name
61388-001	Zingo	lidocaine hydrochloride monohydrate
70645-123	Zingo	lidocaine hydrochloride monohydrate
69420-1230	Lidocaine Hydrochloride Monohydrate	Lidocaine Hydrochloride Monohydrate