NDC 80725-250

Humatin

Paromomycin Sulfate

Humatin is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Waylis Therapeutics Llc. The primary component is Paromomycin Sulfate.

• Product ID: 80725-250_218563ce-a4f4-490b-99fe-eabc713bbdba
• NDC: 80725-250
• Product Type: Human Prescription Drug
• Proprietary Name: Humatin
• Generic Name: Paromomycin Sulfate
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2021-04-08
• Marketing Category: ANDA /
• Application Number: ANDA065173
• Labeler Name: Waylis Therapeutics LLC
• Substance Name: PAROMOMYCIN SULFATE
• Active Ingredient Strength: 250 mg/1
• Pharm Classes: Antiprotozoal [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2024-12-31

Packaging

NDC 80725-250-01

100 CAPSULE in 1 BOTTLE (80725-250-01)

• Marketing Start Date: 2021-04-08
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Humatin" or generic name "Paromomycin Sulfate"

NDC	Brand Name	Generic Name
69784-510	Humatin	PAROMOMYCIN SULFATE
80725-250	Humatin	PAROMOMYCIN SULFATE
23155-038	Paromomycin Sulfate	Paromomycin Sulfate
55695-022	Paromomycin Sulfate	Paromomycin Sulfate
57664-175	Paromomycin Sulfate	Paromomycin Sulfate
76413-147	Paromomycin Sulfate	Paromomycin Sulfate