Home NDC 57664-071 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 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 · 36 matching rows.
View current auxiliary records. · View the auxiliary file history.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded FERROUS SULFATE ACTIVE INGREDIENT 39R4TAN1VT FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 FERROUS CATION ACTIVE MOIETY GW89581OWR FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE INACTIVE INGREDIENT O7TSZ97GEP FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 CARNAUBA WAX INACTIVE INGREDIENT R12CBM0EIZ FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 FD&C BLUE NO. 2 INACTIVE INGREDIENT L06K8R7DQK FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 POLYETHYLENE GLYCOL 8000 INACTIVE INGREDIENT Q662QK8M3B FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 RIBOFLAVIN INACTIVE INGREDIENT TLM2976OFR FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP FERROUS SULFATE TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.] 1
DailyMed RxNorm Mappings#