FOLIC ACID

Product NDC
68071-4175
11-digit product format
680714175
Labeler code
68071
Product ID
68071-4175_bb64231a-3b26-3c15-e053-2a95a90ad079
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
folic acid
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA204418
Marketing category
ANDA
Marketing start
2015-08-04
Marketing end
0000-00-00
Substance
FOLIC ACID
Active strength
1 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-4175-36807141750330 TABLET in 1 BOTTLE (68071-4175-3) 30 tablet2017-12-050000-00-00NoNoCurrent
68071-4175-96807141750990 TABLET in 1 BOTTLE (68071-4175-9) 90 tablet2017-12-050000-00-00NoNoCurrent