Home NDC 42937-705 Prenatal Plus
Product NDC 42937-705
11-digit product format 429370705
Labeler code 42937
Product ID 42937-705_ed67c3cd-b0d8-4a62-90ad-1cf5312de23f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Vitamin A, Ascorbic Acid, Cholecalciferol, .Alpha.-Tocopherol Acetate, Dl-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium Carbonate, Iron, Zinc Oxide, and Cupric Oxide
Dosage form TABLET
Route ORAL
Labeler Nationwide Laboratories
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2011-06-01
Marketing end 0000-00-00
Substance VITAMIN A; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, DL-; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM CARBONATE; IRON; ZINC OXIDE; CUPRIC OXIDE
Active strength 4000 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 42937-705-10 42937070510 100 TABLET in 1 BOTTLE (42937-705-10) 100 tablet 2011-06-01 0000-00-00 No No Current 42937-705-16 42937070516 250 TABLET in 1 BOTTLE (42937-705-16) 250 tablet 2011-06-01 0000-00-00 No No Current 42937-705-18 42937070518 500 TABLET in 1 BOTTLE (42937-705-18) 500 tablet 2011-06-01 0000-00-00 No No Current