testosterone cypionate
Generic: testosterone cypionate
Labeler: american regent, inc.Drug Facts
Product Profile
Brand Name
testosterone cypionate
Generic Name
testosterone cypionate
Labeler
american regent, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
testosterone cypionate 200 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0517-1830
Product ID
0517-1830_110449a6-1353-41e1-a41e-cb4cb4f0a5ae
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207742
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2019-07-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05171830
Hyphenated Format
0517-1830
Supplemental Identifiers
RxCUI
UNII
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
testosterone cypionate (source: ndc)
Generic Name
testosterone cypionate (source: ndc)
Application Number
ANDA207742 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/mL
Packaging
- 1 VIAL in 1 BOX (0517-1830-01) / 1 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "110449a6-1353-41e1-a41e-cb4cb4f0a5ae", "openfda": {"unii": ["M0XW1UBI14"], "rxcui": ["2047882"], "spl_set_id": ["08f88e0e-d9a4-4a03-9286-46d9bf9a363e"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0517-1830-01) / 1 mL in 1 VIAL", "package_ndc": "0517-1830-01", "marketing_start_date": "20190719"}], "brand_name": "Testosterone Cypionate", "product_id": "0517-1830_110449a6-1353-41e1-a41e-cb4cb4f0a5ae", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Androgen Receptor Agonists [MoA]", "Androgen [EPC]", "Androstanes [CS]"], "product_ndc": "0517-1830", "dea_schedule": "CIII", "generic_name": "Testosterone Cypionate", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Testosterone Cypionate", "active_ingredients": [{"name": "TESTOSTERONE CYPIONATE", "strength": "200 mg/mL"}], "application_number": "ANDA207742", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}