FOLIC ACID

Product NDC
70518-0866
11-digit product format
705180866
Labeler code
70518
Product ID
70518-0866_eaff55db-95ad-df69-e053-2995a90a4a87
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
folic acid
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA204418
Marketing category
ANDA
Marketing start
2017-11-24
Marketing end
0000-00-00
Substance
FOLIC ACID
Active strength
1 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-0866FOLIC ACID TABLET [REMEDYREPACK INC.]17Legacy NDC20250503_08bd3640-b14f-4547-93e7-f5641e4c960d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-0866-07051808660030 TABLET in 1 BLISTER PACK (70518-0866-0) 30 tablet2017-11-240000-00-00NoNoCurrent
70518-0866-1705180866017 TABLET in 1 BLISTER PACK (70518-0866-1) 7 tablet2019-12-060000-00-00NoNoCurrent
70518-0866-2705180866027 TABLET in 1 BLISTER PACK (70518-0866-2) 7 tablet2021-03-260000-00-00NoNoCurrent
70518-0866-370518086603100 TABLET in 1 BOTTLE, PLASTIC (70518-0866-3) 100 tablet2021-12-080000-00-00NoNoCurrent
70518-0866-470518086604100 POUCH in 1 BOX (70518-0866-4) > 1 TABLET in 1 POUCH (70518-0866-5) 100 pouch2022-08-010000-00-00NoNoCurrent