testosterone cypionate
Generic: testosterone cypionate
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
testosterone cypionate
Generic Name
testosterone cypionate
Labeler
asclemed usa, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
testosterone cypionate 200 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-752
Product ID
76420-752_1aaa41c9-f5ad-54c2-e063-6394a90a6cc5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207742
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2022-11-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420752
Hyphenated Format
76420-752
Supplemental Identifiers
RxCUI
UNII
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, MULTI-DOSE in 1 CARTON (76420-752-10) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "1aaa41c9-f5ad-54c2-e063-6394a90a6cc5", "openfda": {"unii": ["M0XW1UBI14"], "rxcui": ["835840", "2047882"], "spl_set_id": ["ffb1ae64-9026-44c9-83a0-32058957ecc9"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (76420-752-10) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "76420-752-10", "marketing_start_date": "20240612"}], "brand_name": "testosterone cypionate", "product_id": "76420-752_1aaa41c9-f5ad-54c2-e063-6394a90a6cc5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Androgen Receptor Agonists [MoA]", "Androgen [EPC]", "Androstanes [CS]"], "product_ndc": "76420-752", "dea_schedule": "CIII", "generic_name": "testosterone cypionate", "labeler_name": "Asclemed USA, 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": "20221102", "listing_expiration_date": "20261231"}