What is NDC 52747-711?

52747-711 is the product NDC for Integra F, Ferrous fumarate 62.5 mg/1 + 4 more ingredients capsule, listed with the FDA by U.S. Pharmaceutical Corporation. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Integra F (Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid).

What is the active ingredient?

Ferrous fumarate, Ferrous asparto glycinate, Folic acid, Ascorbic acid, Niacin.

U.S. Pharmaceutical Corporation, NDC labeler code 52747. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Integra F?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Integra F NDC 52747-711 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)52747-711Labeler and product segments. Claims need a package NDC.

Product NDC at billing width52747-0711Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
52747-711-30	5274707113052747071130	30 CAPSULE in 1 BOTTLE, PLASTIC (52747-711-30)Marketed from Apr 27, 2009
52747-711-60	5274707116052747071160	90 CAPSULE in 1 BOTTLE, PLASTIC (52747-711-60)Marketed from Apr 27, 2009

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Integra F
Generic name (nonproprietary): ferrous fumarate and polysacchride iron complex and folic acid
Active ingredients: Ferrous fumarate — 62.5 mg/1Ferrous asparto glycinate — 62.5 mg/1Folic acid — 1 mg/1Ascorbic acid — 40 mg/1Niacin — 3 mg/1
Dosage form: Capsule
Route: Oral
Labeler: U.S. Pharmaceutical CorporationNDC labeler code 52747
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 27, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Ascorbic Acid (Chemical structure)Nicotinic Acids (Chemical structure)
Identifiers: Product ID 52747-711_7aa8c3c6-7a91-4217-9e48-e1dfcf938060SPL ID 7aa8c3c6-7a91-4217-9e48-e1dfcf938060SPL set ID 025fee85-53a8-4161-a806-44fd95d0ca74RxCUI 999823, 999826UNII R5L488RY0Q, H7426RGB3L, 935E97BOY8, PQ6CK8PD0R, 2679MF687A
Pharmacologic class: Nicotinic Acid; Vitamin C

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N452747071130 followed by a unit qualifier and the quantity

Package 52747-0711-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 8, 2022.

Indications (excerpt from the label)

INDICATIONS: Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 52747-711

What is NDC 52747-711?: 52747-711 is the product NDC for Integra F, Ferrous fumarate 62.5 mg/1 + 4 more ingredients capsule, listed with the FDA by U.S. Pharmaceutical Corporation. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Integra F (Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid).
What is the active ingredient?: Ferrous fumarate, Ferrous asparto glycinate, Folic acid, Ascorbic acid, Niacin.
Who is the labeler?: U.S. Pharmaceutical Corporation, NDC labeler code 52747. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Integra F?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.