altachlore sodium chloride hypertonicity

Generic: sodium chloride

Labeler: altaire pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name altachlore sodium chloride hypertonicity
Generic Name sodium chloride
Labeler altaire pharmaceuticals inc.
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

sodium chloride 50 mg/mL

Manufacturer
Altaire Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59390-183
Product ID 59390-183_0c0e9c0d-61f5-e63b-e063-6294a90ac0d9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M018
Listing Expiration 2026-12-31
Marketing Start 2002-09-24

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59390183
Hyphenated Format 59390-183

Supplemental Identifiers

RxCUI
730780
UNII
451W47IQ8X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name altachlore sodium chloride hypertonicity (source: ndc)
Generic Name sodium chloride (source: ndc)
Application Number M018 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (59390-183-13) / 15 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

Ingredients (1)

sodium chloride (50 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "0c0e9c0d-61f5-e63b-e063-6294a90ac0d9", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["730780"], "spl_set_id": ["dc0d94d8-4475-4956-8ded-bdb9496074e4"], "manufacturer_name": ["Altaire Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (59390-183-13)  / 15 mL in 1 BOTTLE, DROPPER", "package_ndc": "59390-183-13", "marketing_start_date": "20020924"}], "brand_name": "Altachlore Sodium Chloride Hypertonicity", "product_id": "59390-183_0c0e9c0d-61f5-e63b-e063-6294a90ac0d9", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "59390-183", "generic_name": "Sodium Chloride", "labeler_name": "Altaire Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Altachlore Sodium Chloride Hypertonicity", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "50 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20020924", "listing_expiration_date": "20261231"}