Home NDC 0409-6660 Sodium Chloride
Product NDC 0409-6660
11-digit product format 004096660
Labeler code 0409
Product ID 0409-6660_c9a3fd1e-32d2-4aa7-bbb4-2852e5c71c8d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name SODIUM CHLORIDE
Dosage form INJECTION, SOLUTION, CONCENTRATE
Route INTRAVENOUS
Labeler Hospira, Inc.
Application NDA018897
Marketing category NDA
Marketing start 2005-07-29
Substance SODIUM CHLORIDE
Active strength 5.84 g/40mL
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0409-6660-25 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0409-6660-25 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 0409-6660-25 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 0409-6660-25 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 0409-6660-25 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 0409-6660-25 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 0409-6660-25 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 0409-6660-25 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 0409-6660-25 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 0409-6660-25 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 0409-6660-25 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 0409-6660-25 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N018897-001 SODIUM CHLORIDE 14.6% SODIUM CHLORIDE 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 N018897-002 SODIUM CHLORIDE 14.6% SODIUM CHLORIDE 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 N018897-003 SODIUM CHLORIDE 23.4% SODIUM CHLORIDE 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
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.
Product history page 1 of 3 · 118 observed 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 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N018897-001 SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 1e350fbaab3a…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 66 observed states.
Additional Listing Data#
Finished product Yes
Brand name base Sodium Chloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 5.84 g/40mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 451W47IQ8X Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1807578 Internal RxNorm lookup 1807580 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 0409-6660-01 Sodium Chloride 40 mL in 1 VIAL INJECTION, SOLUTION, CONCENTRATE 40 24 0409-6660-75 Sodium Chloride 25 in 1 TRAY INJECTION, SOLUTION, CONCENTRATE 25 24
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SODIUM CHLORIDE INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] 14 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 SODIUM CHLORIDE INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] 14 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB SODIUM CHLORIDE INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] 14 WATER INACTIVE INGREDIENT 059QF0KO0R SODIUM CHLORIDE INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0409-6660 SODIUM CHLORIDE INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] 23 Current NDC, Legacy NDC, 2 package rows 20241017_018a8807-1331-41c3-4889-c7ec502a9043.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 · 2 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 0409-6660-01 00409666001 40 mL in 1 VIAL 40 ml Historical 0409-6660-75 00409666075 25 VIAL in 1 TRAY (0409-6660-75) / 40 mL in 1 VIAL (0409-6660-01) 25 vial 2005-07-29 0000-00-00 No No Current