angiotensin ii
Generic: angiotensin ii
Labeler: gland pharma limitedDrug Facts
Product Profile
Brand Name
angiotensin ii
Generic Name
angiotensin ii
Labeler
gland pharma limited
Dosage Form
INJECTION
Routes
Active Ingredients
angiotensin ii 2.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68083-553
Product ID
68083-553_db7a3372-cd0e-412e-a8e2-90b5fdcf3e3e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216966
Listing Expiration
2026-12-31
Marketing Start
2025-06-03
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68083553
Hyphenated Format
68083-553
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
angiotensin ii (source: ndc)
Generic Name
angiotensin ii (source: ndc)
Application Number
ANDA216966 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (68083-553-01) / 1 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "db7a3372-cd0e-412e-a8e2-90b5fdcf3e3e", "openfda": {"nui": ["N0000192562", "N0000009908"], "unii": ["M089EFU921"], "rxcui": ["1999007"], "spl_set_id": ["727d1102-fc46-46f8-b78e-fd13f0738fe4"], "pharm_class_pe": ["Vasoconstriction [PE]"], "pharm_class_epc": ["Vasoconstrictor [EPC]"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (68083-553-01) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68083-553-01", "marketing_start_date": "20250603"}], "brand_name": "ANGIOTENSIN II", "product_id": "68083-553_db7a3372-cd0e-412e-a8e2-90b5fdcf3e3e", "dosage_form": "INJECTION", "pharm_class": ["Vasoconstriction [PE]", "Vasoconstrictor [EPC]"], "product_ndc": "68083-553", "generic_name": "ANGIOTENSIN II", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ANGIOTENSIN II", "active_ingredients": [{"name": "ANGIOTENSIN II", "strength": "2.5 mg/mL"}], "application_number": "ANDA216966", "marketing_category": "ANDA", "marketing_start_date": "20250603", "listing_expiration_date": "20261231"}