NDC 0085-0492

Guanidine hydrochloride

Guanidine Hydrochloride

Guanidine hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Merck Sharp & Dohme Corp.. The primary component is Guanidine Hydrochloride.

• Product ID: 0085-0492_6488a4e4-d1c8-45cb-8fef-48de492e5685
• NDC: 0085-0492
• Product Type: Human Prescription Drug
• Proprietary Name: Guanidine hydrochloride
• Generic Name: Guanidine Hydrochloride
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1939-10-02
• Marketing Category: NDA / NDA
• Application Number: NDA001546
• Labeler Name: Merck Sharp & Dohme Corp.
• Substance Name: GUANIDINE HYDROCHLORIDE
• Active Ingredient Strength: 125 mg/1
• Pharm Classes: Acetylcholine Releasing Agent [EPC],Increased Acetylcholine Activity [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0085-0492-01

100 TABLET in 1 BOTTLE (0085-0492-01)

• Marketing Start Date: 1939-10-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0085-0492-01 [00085049201]

Guanidine hydrochloride TABLET

• Marketing Category: NDA
• Application Number: NDA001546
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1939-10-02

Drug Details

Active Ingredients

Ingredient	Strength
GUANIDINE HYDROCHLORIDE	125 mg/1

OpenFDA Data

• SPL SET ID: 903fbd33-e5d9-41fb-9414-7bd6f42a8593
• Manufacturer:
  • Merck Sharp & Dohme Corp.
• UNII:
  • 3YQC9ZY4YB
• RxNorm Concept Unique ID - RxCUI:
  • 1298099
• UPC Code:
  • 0300850492018

Pharmacological Class

• Acetylcholine Releasing Agent [EPC]
• Increased Acetylcholine Activity [PE]