HYDROCORTISONE MAXIMUM STRENGTH

Product NDC
70403-922
11-digit product format
704030922
Labeler code
70403
Product ID
70403-922_b2daf4b9-f797-4467-b77f-43836f7e3ccb
Type
HUMAN OTC DRUG
Nonproprietary name
Hydrocortisone
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Aru Pharma Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-01-01
Marketing end
0000-00-00
Substance
HYDROCORTISONE
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70403-922-30GM - Gram70403-9221376ab2f-fb77-4917-a279-e9bab68d39c112020-01-03