NDC 59088-749

Lidotin

Gabapentin, Lidocaine Hydrochloride

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

• Product ID: 59088-749_9fe6a816-38c1-ef66-e053-2a95a90aa41d
• NDC: 59088-749
• Product Type: Human Prescription Drug
• Proprietary Name: Lidotin
• Generic Name: Gabapentin, Lidocaine Hydrochloride
• Dosage Form: Kit
• Marketing Start Date: 2020-03-02
• Marketing Category: ANDA / ANDA
• Application Number: ANDA204989
• Labeler Name: PureTek Corporation
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 59088-749-00

1 KIT in 1 CARTON (59088-749-00) * 24 CAPSULE in 1 BOTTLE (50436-0383-4) * 1 TUBE in 1 CARTON (59088-371-07) > 85 g in 1 TUBE

• Marketing Start Date: 2020-03-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59088-749-00 [59088074900]

Lidotin KIT

• Marketing Category: ANDA
• Application Number: ANDA204989
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-03-02

Drug Details

OpenFDA Data

• SPL SET ID: 9fe6a350-43be-9db8-e053-2995a90aaa6e
• Manufacturer:
  • PureTek Corporation
• RxNorm Concept Unique ID - RxCUI:
  • 1723996
  • 310430
  • 1723991

NDC Crossover Matching brand name "Lidotin" or generic name "Gabapentin, Lidocaine Hydrochloride"

NDC	Brand Name	Generic Name
59088-749	Lidotin	GABAPENTIN, LIDOCAINE HYDROCHLORIDE
59088-747	GABAPAL	GABAPENTIN, LIDOCAINE HYDROCHLORIDE
59088-736	GPL Pak	GABAPENTIN, LIDOCAINE HYDROCHLORIDE
59088-743	Lido GB-300	GABAPENTIN, LIDOCAINE HYDROCHLORIDE