vasopressin
Generic: vasopressin
Labeler: amphastar pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
vasopressin
Generic Name
vasopressin
Labeler
amphastar pharmaceuticals, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
vasopressin 20 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0548-9701
Product ID
0548-9701_93e40d97-9476-44dc-80dc-4c9d33062d63
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211857
Listing Expiration
2026-12-31
Marketing Start
2022-08-22
Pharmacologic Class
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05489701
Hyphenated Format
0548-9701
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA211857 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 [USP'U]/mL
Packaging
- 1 VIAL in 1 CARTON (0548-9701-00) / 1 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "93e40d97-9476-44dc-80dc-4c9d33062d63", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "unii": ["Y4907O6MFD"], "rxcui": ["2103182"], "spl_set_id": ["4e6c737d-65e8-4af4-b301-69a93affbc7f"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["Amphastar Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0548-9701-00) / 1 mL in 1 VIAL", "package_ndc": "0548-9701-00", "marketing_start_date": "20220831"}], "brand_name": "Vasopressin", "product_id": "0548-9701_93e40d97-9476-44dc-80dc-4c9d33062d63", "dosage_form": "INJECTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "0548-9701", "generic_name": "Vasopressin", "labeler_name": "Amphastar Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vasopressin", "active_ingredients": [{"name": "VASOPRESSIN", "strength": "20 [USP'U]/mL"}], "application_number": "ANDA211857", "marketing_category": "ANDA", "marketing_start_date": "20220822", "listing_expiration_date": "20261231"}