vasopressin

Generic: vasopressin

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vasopressin
Generic Name vasopressin
Labeler amneal pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

vasopressin 20 [USP'U]/mL

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 70121-1642
Product ID 70121-1642_852dfca1-d3f4-4c85-8140-1b74e464ec0c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212944
Listing Expiration 2026-12-31
Marketing Start 2022-08-11

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 701211642
Hyphenated Format 70121-1642

Supplemental Identifiers

RxCUI
2103182
UPC
0370121164258 0370121164210 0370121164272
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 (source: ndc)
Generic Name vasopressin (source: ndc)
Application Number ANDA212944 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 [USP'U]/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (70121-1642-2) / 1 mL in 1 VIAL (70121-1642-1)
  • 25 VIAL in 1 CARTON (70121-1642-5) / 1 mL in 1 VIAL (70121-1642-1)
  • 10 VIAL in 1 CARTON (70121-1642-7) / 1 mL in 1 VIAL (70121-1642-1)
source: ndc

Packages (3)

70121-1642-2 1 VIAL in 1 CARTON (70121-1642-2) / 1 mL in 1 VIAL (70121-1642-1) 70121-1642-5 25 VIAL in 1 CARTON (70121-1642-5) / 1 mL in 1 VIAL (70121-1642-1) 70121-1642-7 10 VIAL in 1 CARTON (70121-1642-7) / 1 mL in 1 VIAL (70121-1642-1)

Ingredients (1)

vasopressin (20 [USP'U]/mL)

Linked Drug Pages (1)

vasopressin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "852dfca1-d3f4-4c85-8140-1b74e464ec0c", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "upc": ["0370121164258", "0370121164210", "0370121164272"], "unii": ["Y4907O6MFD"], "rxcui": ["2103182"], "spl_set_id": ["d9869345-b02c-4225-a97b-656f14c86dec"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70121-1642-2)  / 1 mL in 1 VIAL (70121-1642-1)", "package_ndc": "70121-1642-2", "marketing_start_date": "20220811"}, {"sample": false, "description": "25 VIAL in 1 CARTON (70121-1642-5)  / 1 mL in 1 VIAL (70121-1642-1)", "package_ndc": "70121-1642-5", "marketing_start_date": "20220811"}, {"sample": false, "description": "10 VIAL in 1 CARTON (70121-1642-7)  / 1 mL in 1 VIAL (70121-1642-1)", "package_ndc": "70121-1642-7", "marketing_start_date": "20220811"}], "brand_name": "vasopressin", "product_id": "70121-1642_852dfca1-d3f4-4c85-8140-1b74e464ec0c", "dosage_form": "INJECTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "70121-1642", "generic_name": "vasopressin", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vasopressin", "active_ingredients": [{"name": "VASOPRESSIN", "strength": "20 [USP'U]/mL"}], "application_number": "ANDA212944", "marketing_category": "ANDA", "marketing_start_date": "20220811", "listing_expiration_date": "20261231"}