NDC 58809-888

Escavite

Sodium Fluoride, Vitamin A Acetate, Biotin, Magnesium, Zinc, Copper, Calcium Pantothenate, Folic Acid, Iron, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, And Cyanocobalamin

Escavite is a Oral Tablet, Chewable in the Human Prescription Drug category. It is labeled and distributed by Gm Pharmaceuticals, Inc.. The primary component is Sodium Fluoride; Vitamin A Acetate; Biotin; Magnesium; Zinc; Copper; Calcium Pantothenate; Folic Acid; Iron; Ascorbic Acid; Cholecalciferol; .alpha.-tocopherol Acetate; Thiamine Mononitrate; Riboflavin; Niacinamide; Pyridoxine Hydrochloride; Cyanocobalamin.

• Product ID: 58809-888_935bc301-7376-4676-8ba5-085e4463e5a2
• NDC: 58809-888
• Product Type: Human Prescription Drug
• Proprietary Name: Escavite
• Generic Name: Sodium Fluoride, Vitamin A Acetate, Biotin, Magnesium, Zinc, Copper, Calcium Pantothenate, Folic Acid, Iron, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, And Cyanocobalamin
• Dosage Form: Tablet, Chewable
• Route of Administration: ORAL
• Marketing Start Date: 2012-02-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: GM Pharmaceuticals, Inc.
• Substance Name: SODIUM FLUORIDE; VITAMIN A ACETATE; BIOTIN; MAGNESIUM; ZINC; COPPER; CALCIUM PANTOTHENATE; FOLIC ACID; IRON; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN
• Active Ingredient Strength: 0 mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; ug/1
• Pharm Classes: Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 58809-888-01

100 TABLET, CHEWABLE in 1 BOTTLE (58809-888-01)

• Marketing Start Date: 2012-02-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58809-888-01 [58809088801]

Escavite TABLET, CHEWABLE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-02-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM FLUORIDE	.25 mg/1

OpenFDA Data

• SPL SET ID: 218eecd3-70a9-4496-8f01-9d7b7897b251
• Manufacturer:
  • GM Pharmaceuticals, Inc.
• UNII:
  • 25X51I8RD4
  • I38ZP9992A
  • 68Y4CF58BV
  • J41CSQ7QDS
  • 568ET80C3D
  • PQ6CK8PD0R
  • 789U1901C5
  • 9E8X80D2L0
  • E1UOL152H7
  • 3LE3D9D6OY
  • 8ZYQ1474W7
  • TLM2976OFR
  • 8K0I04919X
  • 935E97BOY8
  • P6YC3EG204
  • 6SO6U10H04
  • 1C6V77QF41

Pharmacological Class

• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]
• Vitamin A [CS]
• Vitamin A [EPC]
• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Vitamin D [CS]
• Vitamin D [EPC]

Medicade Reported Pricing

58809088801 ESCAVITE TABLET CHEWABLE

Pricing Unit: EA | Drug Type: