NDC 0642-0072

Vitafol Caplet

Vitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, And Iron

Vitafol Caplet is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Everett Laboratories, Inc.. The primary component is Vitamin A; Ascorbic Acid; Vitamin D; .alpha.-tocopherol; Thiamine Mononitrate; Riboflavin; Niacin; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Calcium; Iron.

• Product ID: 0642-0072_667440e5-a115-41f7-91a7-8acf0edc115f
• NDC: 0642-0072
• Product Type: Human Prescription Drug
• Proprietary Name: Vitafol Caplet
• Generic Name: Vitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, And Iron
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1985-05-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Everett Laboratories, Inc.
• Substance Name: VITAMIN A; ASCORBIC ACID; VITAMIN D; .ALPHA.-TOCOPHEROL; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM; IRON
• Active Ingredient Strength: 6000 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1
• Pharm Classes: Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Calcium [CS],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0642-0072-12

100 CAPSULE in 1 BOX (0642-0072-12)

• Marketing Start Date: 1985-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0642-0072-12 [00642007212]

Vitafol Caplet CAPSULE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1985-05-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
VITAMIN A	6000 [iU]/1

OpenFDA Data

• SPL SET ID: d4713072-1864-40ce-b003-a171fb2bc127
• Manufacturer:
  • Everett Laboratories, Inc.
• UNII:
  • SY7Q814VUP
  • 68Y4CF58BV
  • PQ6CK8PD0R
  • E1UOL152H7
  • 9VU1KI44GP
  • TLM2976OFR
  • 2679MF687A
  • 8K0I04919X
  • 935E97BOY8
  • H4N855PNZ1
  • 81G40H8B0T
  • P6YC3EG204

Pharmacological Class

• Vitamin A [CS]
• Vitamin A [EPC]
• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Vitamin D [CS]
• Vitamin D [EPC]
• Nicotinic Acid [EPC]
• Nicotinic Acids [CS]
• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]
• Calcium [CS]
• Calcium [EPC]
• Phosphate Binder [EPC]
• Phosphate Chelating Activity [MoA]