NDC 52747-712

Integra Plus

Ferrous Fumarate And Polysacchride Iron Vitamin Mineral Complex Supplement

Integra Plus is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by U.s. Pharmaceutical Corporation. The primary component is Ascorbic Acid; Biotin; Calcium Pantothenate; Ferrous Asparto Glycinate; Ferrous Fumarate; Folic Acid; Niacin; Pyridoxine Hydrochloride; Riboflavin; Thiamine Mononitrate.

• Product ID: 52747-712_61ed22a2-e729-482f-aa6c-47932798bccc
• NDC: 52747-712
• Product Type: Human Prescription Drug
• Proprietary Name: Integra Plus
• Generic Name: Ferrous Fumarate And Polysacchride Iron Vitamin Mineral Complex Supplement
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2009-04-27
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: U.S. Pharmaceutical Corporation
• Substance Name: ASCORBIC ACID; BIOTIN; CALCIUM PANTOTHENATE; FERROUS ASPARTO GLYCINATE; FERROUS FUMARATE; FOLIC ACID; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE
• Active Ingredient Strength: 210 mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
• Pharm Classes: Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Nicotinic Acid [EPC], Nicotinic Acids [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 52747-712-10

40 BLISTER PACK in 1 BOX (52747-712-10) > 4 BOTTLE, PLASTIC in 1 BLISTER PACK (52747-712-04) > 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-712-60)

• Marketing Start Date: 2009-04-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52747-712-10 [52747071210]

Integra Plus CAPSULE

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-27
• Inactivation Date: 2019-10-21

NDC 52747-712-60 [52747071260]

Integra Plus CAPSULE

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-04-27

NDC 52747-712-04 [52747071204]

Integra Plus CAPSULE

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-27

Drug Details

Active Ingredients

Ingredient	Strength
FERROUS FUMARATE	191.2 mg/1

OpenFDA Data

• SPL SET ID: 9e5b9309-e835-4863-ab6f-e3018e38fc64
• Manufacturer:
  • US Pharmaceutical Corporation
• UNII:
  • R5L488RY0Q
  • 568ET80C3D
  • 2679MF687A
  • H7426RGB3L
  • 68Y4CF58BV
  • TLM2976OFR
  • PQ6CK8PD0R
  • 8K0I04919X
  • 935E97BOY8
  • 6SO6U10H04

Pharmacological Class

• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Nicotinic Acid [EPC]
• Nicotinic Acids [CS]
• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]

Medicade Reported Pricing

52747071260 INTEGRA PLUS CAPSULE

Pricing Unit: EA | Drug Type:

52747071230 INTEGRA PLUS CAPSULE

Pricing Unit: EA | Drug Type: