Home NDC 65219-274 Succinylcholine Chloride
Product NDC 65219-274
11-digit product format 652190274
Labeler code 65219
Product ID 65219-274_7652543e-1b4b-40b9-8bc3-6fde0ec823ae
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Succinylcholine Chloride
Dosage form INJECTION, SOLUTION
Route INTRAMUSCULAR; INTRAVENOUS
Labeler Fresenius Kabi USA LLC
Application ANDA217884
Marketing category ANDA
Marketing start 2025-06-19
Substance SUCCINYLCHOLINE CHLORIDE DIHYDRATE
Active strength 20 mg/mL
Pharmacologic classes Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A217884-001 SUCCINYLCHOLINE CHLORIDE SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP RS 2025-02-11
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A217884-001 AP
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-18 06:07:40 2026-07 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP RS 2025-02-11 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP 2025-02-11 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP 2025-02-11 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP 2025-02-11 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP 2025-02-11 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP 2025-02-11 b8a1b40f171c…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A217884-001 SUCCINYLCHOLINE CHLORIDE 100MG/5ML (20MG/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS AP RS 2025-02-11 a50c72e98297…
Observed Orange Book normalized TE history# Additional Listing Data#
Finished product Yes
Brand name base Succinylcholine Chloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SUCCINYLCHOLINE CHLORIDE DIHYDRATE 20 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8L0S1G435E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2598128 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 65219-274-01 Succinylcholine Chloride 5 mL in 1 SYRINGE, PLASTIC INJECTION, SOLUTION 5 8 65219-274-05 Succinylcholine Chloride 10 in 1 CARTON INJECTION, SOLUTION 10 8
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 Sample Exclude flag Status 65219-274-01 65219027401 5 mL in 1 SYRINGE, PLASTIC 5 ml Historical 65219-274-05 65219027405 10 SYRINGE, PLASTIC in 1 CARTON (65219-274-05) / 5 mL in 1 SYRINGE, PLASTIC (65219-274-01) 2025-06-19 No No Current