Ferrous Sulfate

Product NDC
57664-071
11-digit product format
576640071
Labeler code
57664
Product ID
57664-071_bca6e06f-e9ea-4957-af87-453044fbf10b
Type
HUMAN OTC DRUG
Nonproprietary name
Ferrous Sulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sun Pharmaceutical Industries, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-07-01
Marketing end
0000-00-00
Substance
FERROUS SULFATE
Active strength
325 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57664-071-01EA - Each57664-0716ebb4586-ec2f-4e6f-9698-a8bcf4b5cdf812015-01-05
57664-071-10EA - Each57664-0713c82e928-f3ca-4389-998d-1e65681d978212015-01-05

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310325ferrous sulfate 325 MG (iron 65 MG) Oral TabletPSNc57a8573-d5ae-48b2-afb7-bbec2f63afff1
310325ferrous sulfate 325 MG Oral TabletSCDc57a8573-d5ae-48b2-afb7-bbec2f63afff1
310325ferrous sulfate 324 MG (iron 65 MG) Oral TabletSYc57a8573-d5ae-48b2-afb7-bbec2f63afff1
310325ferrous sulfate 325 MG (iron 65 MG) Oral TabletSYc57a8573-d5ae-48b2-afb7-bbec2f63afff1
310325FESO4 325 MG Oral TabletSYc57a8573-d5ae-48b2-afb7-bbec2f63afff1