Home NDC 0409-1141-02 SODIUM CHLORIDE
Product NDC 0409-1141
Requested package NDC 0409-1141-02
11-digit product format 004091141
Labeler code 0409
Product ID 0409-1141_4b8e6f49-4268-4654-9b7d-8dcd235aa040
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 2005-04-30
Substance SODIUM CHLORIDE
Active strength 234 mg/mL
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 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
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14.6% SODIUM CHLORIDE 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 N018897-002 SODIUM CHLORIDE 14.6% SODIUM CHLORIDE 100MEQ/40ML (2.5MEQ/ML) SOLUTION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 4 · 121 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 2026-09-14 22:38:34 2026-08 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SODIUM CHLORIDE 14.6% 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** SOLUTION / INTRAVENOUS RLD 1984-07-20 84e616aacf4f…2026-09-14 22:38:34 2026-08 N018897-002 SODIUM CHLORIDE 14.6% 100MEQ/40ML (2.5MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 1984-07-20 84e616aacf4f…2026-09-14 22:38:34 2026-08 N018897-003 SODIUM CHLORIDE 23.4% 400MEQ/100ML (4MEQ/ML) SOLUTION / INTRAVENOUS AP RLD, RS 2020-06-18 84e616aacf4f…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…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 68 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base SODIUM CHLORIDE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 234 mg/mL
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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313016 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 0409-1141-02 SODIUM CHLORIDE 25 in 1 CASE INJECTION, SOLUTION, CONCENTRATE 25 8 0409-1141-12 SODIUM CHLORIDE 100 mL in 1 VIAL, PHARMACY BULK PACKAGE INJECTION, SOLUTION, CONCENTRATE 100 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SODIUM CHLORIDE INJECTION, SOLUTION [HOSPIRA, INC.] 2 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 SODIUM CHLORIDE INJECTION, SOLUTION [HOSPIRA, INC.] 2 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB SODIUM CHLORIDE INJECTION, SOLUTION [HOSPIRA, INC.] 2 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I SODIUM CHLORIDE INJECTION, SOLUTION [HOSPIRA, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0409-1141 SODIUM CHLORIDE INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] 7 Current NDC, Legacy NDC, 2 package rows 20241109_af6aebad-ef03-4d19-9a40-18e5a278b812.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 Marketing start Marketing end Sample Exclude flag Status 0409-1141-02 00409114102 25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12) 2005-04-30 0000-00-00 No No Current