NDC 59088-747

GABAPAL

Gabapentin, Lidocaine Hydrochloride

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

• Product ID: 59088-747_9cfd2461-a093-7f17-e053-2a95a90abbd3
• NDC: 59088-747
• Product Type: Human Prescription Drug
• Proprietary Name: GABAPAL
• Generic Name: Gabapentin, Lidocaine Hydrochloride
• Dosage Form: Kit
• Route of Administration: ORAL; TOPICAL
• Marketing Start Date: 2020-01-25
• 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 59088-747-00

1 KIT in 1 CARTON (59088-747-00) * 24 CAPSULE in 1 BOTTLE * 1 TUBE in 1 CARTON (59088-371-07) > 85 g in 1 TUBE

• Marketing Start Date: 2020-02-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59088-747-00 [59088074700]

GABAPAL KIT

• Marketing Category: ANDA
• Application Number: ANDA204989
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-02-01

Drug Details

OpenFDA Data

• SPL SET ID: 9cfd2461-a092-7f17-e053-2a95a90abbd3
• Manufacturer:
  • PureTek Corporation
• RxNorm Concept Unique ID - RxCUI:
  • 1723996
  • 310430
  • 1723991

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

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