NDC 67555-140

MaxFe

Ascorbic Acid, Folic Acid, Vitamin B-12, Biotin, Iron, Magnesium, Zinc

MaxFe is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pronova Corporation. The primary component is Ascorbic Acid; Folic Acid; Cyanocobalamin; Biotin; Iron; Magnesium; Zinc; Docusate Sodium.

• Product ID: 67555-140_a769b672-5a74-4d2a-a01a-e7c3c124d94e
• NDC: 67555-140
• Product Type: Human Prescription Drug
• Proprietary Name: MaxFe
• Generic Name: Ascorbic Acid, Folic Acid, Vitamin B-12, Biotin, Iron, Magnesium, Zinc
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-06-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Pronova Corporation
• Substance Name: ASCORBIC ACID; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; IRON; MAGNESIUM; ZINC; DOCUSATE SODIUM
• Active Ingredient Strength: 100 mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1
• Pharm Classes: Vitamin C [EPC],Ascorbic Acid [CS],Vitamin B 12 [CS],Vitamin B12 [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 67555-140-12

120 TABLET in 1 BOTTLE (67555-140-12)

• Marketing Start Date: 2014-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 67555-140-12 [67555014012]

MaxFe TABLET

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-06-01
• Marketing End Date: 2020-01-01
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-02-18

Drug Details

Active Ingredients

Ingredient	Strength
ASCORBIC ACID	100 mg/1

OpenFDA Data

• SPL SET ID: 0883e94f-7987-4a17-a7c1-70655d827c17
• Manufacturer:
  • Pronova Corporation
• UNII:
  • J41CSQ7QDS
  • PQ6CK8PD0R
  • E1UOL152H7
  • I38ZP9992A
  • 935E97BOY8
  • F05Q2T2JA0
  • 6SO6U10H04
  • P6YC3EG204
• UPC Code:
  • 0367555140125

Pharmacological Class

• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]