NDC 0220-1335

Cholesterinum

Cholesterol

Cholesterinum is a Oral Pellet in the Human Prescription Drug category. It is labeled and distributed by Boiron. The primary component is Cholesterol.

• Product ID: 0220-1335_852974e2-fded-d91c-e053-2a91aa0a108d
• NDC: 0220-1335
• Product Type: Human Prescription Drug
• Proprietary Name: Cholesterinum
• Generic Name: Cholesterol
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: CHOLESTEROL
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-1335-41

30 [hp_C] in 1 TUBE (0220-1335-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-1335-41 [00220133541]

Cholesterinum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
CHOLESTEROL	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 852974e2-fdec-d91c-e053-2a91aa0a108d
• Manufacturer:
  • Boiron
• UNII:
  • 97C5T2UQ7J

NDC Crossover Matching brand name "Cholesterinum" or generic name "Cholesterol"

NDC	Brand Name	Generic Name
0220-1334	Cholesterinum	CHOLESTEROL
0220-1335	Cholesterinum	CHOLESTEROL
0220-1339	Cholesterinum	CHOLESTEROL
0220-1341	Cholesterinum	CHOLESTEROL
15631-0132	CHOLESTERINUM	CHOLESTERINUM
62106-5732	CHOLESTERINUM	Cholesterine
68428-315	Cholesterinum	CHOLESTEROL
71919-194	Cholesterinum	CHOLESTEROL
43742-0562	CHOLESTEROL	Cholesterinum
43742-1272	Cholesterol	Cholesterinum
63083-1551	Cholesterol	Cholesterol