vasopressin in 0.9% sodium chloride

Generic: vasopressin

Labeler: long grove pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name vasopressin in 0.9% sodium chloride
Generic Name vasopressin
Labeler long grove pharmaceuticals, llc
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vasopressin .2 [USP'U]/mL

Manufacturer
Long Grove Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 81298-8552
Product ID 81298-8552_55507afe-de33-407d-bf9d-1b916efa1518
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA217766
Listing Expiration 2026-12-31
Marketing Start 2024-07-12

Pharmacologic Class

Chemical Structure
vasopressins [cs]
Physiologic Effect
vasoconstriction [pe] decreased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 812988552
Hyphenated Format 81298-8552

Supplemental Identifiers

RxCUI
2399907 2591428
UPC
0381298855238 0381298855436
UNII
Y4907O6MFD
NUI
M0022562 N0000009908 N0000175360

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 vasopressin in 0.9% sodium chloride (source: ndc)
Generic Name vasopressin (source: ndc)
Application Number NDA217766 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .2 [USP'U]/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (81298-8552-3) / 100 mL in 1 VIAL, SINGLE-DOSE (81298-8552-1)
source: ndc

Packages (1)

Ingredients (1)

vasopressin (.2 [USP'U]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "55507afe-de33-407d-bf9d-1b916efa1518", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "upc": ["0381298855238", "0381298855436"], "unii": ["Y4907O6MFD"], "rxcui": ["2399907", "2591428"], "spl_set_id": ["bf4b0b63-0055-40d8-b331-7f9f1ea3214c"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["Long Grove Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (81298-8552-3)  / 100 mL in 1 VIAL, SINGLE-DOSE (81298-8552-1)", "package_ndc": "81298-8552-3", "marketing_start_date": "20240712"}], "brand_name": "Vasopressin in 0.9% Sodium Chloride", "product_id": "81298-8552_55507afe-de33-407d-bf9d-1b916efa1518", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "81298-8552", "generic_name": "Vasopressin", "labeler_name": "Long Grove Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vasopressin in 0.9% Sodium Chloride", "active_ingredients": [{"name": "VASOPRESSIN", "strength": ".2 [USP'U]/mL"}], "application_number": "NDA217766", "marketing_category": "NDA", "marketing_start_date": "20240712", "listing_expiration_date": "20261231"}