Home NDC 65044-9998 Positive Skin Test Control - Histamine
Product NDC 65044-9998
11-digit product format 650449998
Labeler code 65044
Product ID 65044-9998_2d00bd89-9169-4cb8-8685-767985bb7908
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Histamine
Dosage form INJECTION
Route PERCUTANEOUS
Labeler Jubilant HollisterStier LLC
Application BLA103891
Marketing category BLA
Marketing start 1995-06-15
Substance HISTAMINE
Active strength 6 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Positive Skin Test Control - Histamine
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HISTAMINE 6 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 820484N8I3 Internal UNII 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 65044-9998-1 Positive Skin Test Control - Histamine 5 mL in 1 VIAL INJECTION 5 16
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65044-9998 POSITIVE SKIN TEST CONTROL - HISTAMINE (HISTAMINE) INJECTION [JUBILANT HOLLISTERSTIER LLC] 14 Current NDC, Legacy NDC, 1 package rows 20241031_5c20f3f4-65f8-4cdb-bdd1-5774da1c551b.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.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 103891 Positive Skin Test Control-Histamine 351(a) Rx 2026-06-01
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 65044-9998-1 65044999801 5 mL in 1 VIAL (65044-9998-1) 5 ml 1995-06-15 0000-00-00 No No Current