Home NDC 16477-201-12 Hemmorex-HC
Product NDC 16477-201
Requested package NDC 16477-201-12
11-digit product format 164770201
Labeler code 16477
Product ID 16477-201_2c65695c-de02-6fa3-e063-6294a90aee9d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name hydrocortisone acetate
Dosage form SUPPOSITORY
Route RECTAL
Labeler Laser Pharmaceuticals, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2013-11-12
Substance HYDROCORTISONE ACETATE
Active strength 25 mg/1
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Hemmorex-HC
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE ACETATE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3X7931PO74 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1291082 Internal RxNorm lookup 1674197 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 16477-201-12 Hemmorex-HC 6 in 1 BLISTER PACK SUPPOSITORY 6 9 16477-201-12 Hemmorex-HC 2 in 1 BOX SUPPOSITORY 2 9 16477-201-24 Hemmorex-HC 6 in 1 BLISTER PACK SUPPOSITORY 6 9 16477-201-24 Hemmorex-HC 4 in 1 BOX SUPPOSITORY 4 9 16477-201-99 Hemmorex-HC 100 in 1 BOX SUPPOSITORY 100 9 16477-201-99 Hemmorex-HC 1 in 1 BLISTER PACK SUPPOSITORY 1 9
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 16477-201 HEMMOREX-HC (HYDROCORTISONE ACETATE) SUPPOSITORY [LASER PHARMACEUTICALS, LLC] 9 Current NDC, Legacy NDC, 6 package rows 20250125_db67f724-c78c-4280-9c2e-6abbaeaef42d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 16477-201-12 16477020112 2 BLISTER PACK in 1 BOX (16477-201-12) / 6 SUPPOSITORY in 1 BLISTER PACK 2 blister pack 2013-11-12 0000-00-00 No No Current