Home NDC 52747-711-60 Integra F
Product NDC 52747-711
Requested package NDC 52747-711-60
11-digit product format 527470711
Labeler code 52747
Product ID 52747-711_7aa8c3c6-7a91-4217-9e48-e1dfcf938060
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid
Dosage form CAPSULE
Route ORAL
Labeler U.S. Pharmaceutical Corporation
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2009-04-27
Substance FERROUS FUMARATE; FERROUS ASPARTO GLYCINATE; FOLIC ACID; ASCORBIC ACID; NIACIN
Active strength 62.5; 62.5; 1; 40; 3 mg/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes Ascorbic Acid [CS], Nicotinic Acid [EPC], Nicotinic Acids [CS], Vitamin C [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Integra F
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERROUS FUMARATE 62.5 mg/1 FERROUS ASPARTO GLYCINATE 62.5 mg/1 FOLIC ACID 1 mg/1 ASCORBIC ACID 40 mg/1 NIACIN 3 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 999823 Internal RxNorm lookup 999826 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52747-711-30 Integra F 30 in 1 BOTTLE, PLASTIC CAPSULE 30 5 52747-711-60 Integra F 90 in 1 BOTTLE, PLASTIC CAPSULE 90 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52747-711 INTEGRA F (FERROUS FUMARATE AND POLYSACCHRIDE IRON COMPLEX AND FOLIC ACID) CAPSULE [U.S. PHARMACEUTICAL CORPORATION] 5 Current NDC, Legacy NDC, 2 package rows 20221110_025fee85-53a8-4161-a806-44fd95d0ca74.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52747-711-60 52747071160 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-711-60) 90 capsule 2009-04-27 0000-00-00 No No Current