FOLIC ACID

Product NDC
68788-7877
11-digit product format
687887877
Labeler code
68788
Product ID
68788-7877_320b8a85-337b-4aea-b6cc-04640683d8ae
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FOLIC ACID
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA040796
Marketing category
ANDA
Marketing start
2021-03-08
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 Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-7877FOLIC ACID TABLET [PREFERRED PHARMACEUTICALS INC.]4Legacy NDC20240504_abd88aaa-6383-43a7-b0a9-a265af302419.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7877-168788787701100 TABLET in 1 BOTTLE (68788-7877-1) 100 tablet2021-03-080000-00-00NoNoCurrent
68788-7877-36878878770330 TABLET in 1 BOTTLE (68788-7877-3) 30 tablet2021-03-080000-00-00NoNoCurrent
68788-7877-66878878770660 TABLET in 1 BOTTLE (68788-7877-6) 60 tablet2021-03-080000-00-00NoNoCurrent
68788-7877-96878878770990 TABLET in 1 BOTTLE (68788-7877-9) 90 tablet2021-03-080000-00-00NoNoCurrent