Home NDC 51662-1439 PHYSOSTIGMINE SALICYLATE
Product NDC 51662-1439
11-digit product format 516621439
Labeler code 51662
Product ID 51662-1439_f1deeef3-92c7-a88e-e053-2a95a90a74a3
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name PHYSOSTIGMINE SALICYLATE
Dosage form INJECTION
Route INTRAVENOUS
Labeler HF Acquisition Co LLC, DBA HealthFirst
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-12-22
Substance PHYSOSTIGMINE SALICYLATE
Active strength 1 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base PHYSOSTIGMINE SALICYLATE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHYSOSTIGMINE SALICYLATE 1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2046ZRO9VU Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 990982 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51662-1439-1 PHYSOSTIGMINE SALICYLATE 2 mL in 1 AMPULE INJECTION 2 3 51662-1439-2 PHYSOSTIGMINE SALICYLATE 2 mL in 1 AMPULE INJECTION 2 3 51662-1439-2 PHYSOSTIGMINE SALICYLATE 1 in 1 POUCH INJECTION 1 3 51662-1439-3 PHYSOSTIGMINE SALICYLATE 10 in 1 CASE INJECTION 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51662-1439 PHYSOSTIGMINE SALICYLATE INJECTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] 3 Current NDC, Legacy NDC, 4 package rows 20230111_9a448a78-356c-50f7-e053-2995a90adefa.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 51662-1439-1 51662143901 2 mL in 1 AMPULE (51662-1439-1) 2 ml 2019-12-22 0000-00-00 No No Current 51662-1439-2 51662143902 2 mL in 1 AMPULE 2 ml Historical 51662-1439-3 51662143903 10 POUCH in 1 CASE (51662-1439-3) / 1 AMPULE in 1 POUCH (51662-1439-2) / 2 mL in 1 AMPULE 10 pouch 2023-01-09 0000-00-00 No No Current