testosterone cypionate
Generic: testosterone cypionate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
testosterone cypionate
Generic Name
testosterone cypionate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
testosterone cypionate 200 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
62756-015
Product ID
62756-015_bf24bb84-d12f-44e7-98bd-46f3aa792bcc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201720
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2013-06-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62756015
Hyphenated Format
62756-015
Supplemental Identifiers
RxCUI
UPC
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
ANDA201720 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/mL
Packaging
- 1 VIAL in 1 CARTON (62756-015-40) / 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": "bf24bb84-d12f-44e7-98bd-46f3aa792bcc", "openfda": {"upc": ["0362756017405", "0362756015401", "0362756016408"], "unii": ["M0XW1UBI14"], "rxcui": ["835829", "835840", "2047882"], "spl_set_id": ["3653a602-4551-4e6c-84a7-31861f5dc482"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (62756-015-40) / 1 mL in 1 VIAL", "package_ndc": "62756-015-40", "marketing_start_date": "20130617"}], "brand_name": "Testosterone Cypionate", "product_id": "62756-015_bf24bb84-d12f-44e7-98bd-46f3aa792bcc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Androgen Receptor Agonists [MoA]", "Androgen [EPC]", "Androstanes [CS]"], "product_ndc": "62756-015", "dea_schedule": "CIII", "generic_name": "Testosterone Cypionate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Testosterone Cypionate", "active_ingredients": [{"name": "TESTOSTERONE CYPIONATE", "strength": "200 mg/mL"}], "application_number": "ANDA201720", "marketing_category": "ANDA", "marketing_start_date": "20130617", "listing_expiration_date": "20261231"}