testosterone cypionate

Generic: testosterone cypionate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name testosterone cypionate
Generic Name testosterone cypionate
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

testosterone cypionate 200 mg/mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-016
Product ID 62756-016_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
androgen receptor agonists [moa] androgen [epc] androstanes [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756016
Hyphenated Format 62756-016

Supplemental Identifiers

RxCUI
835829 835840 2047882
UPC
0362756017405 0362756015401 0362756016408
UNII
M0XW1UBI14

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (62756-016-40) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

Ingredients (1)

testosterone cypionate (200 mg/mL)

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, MULTI-DOSE in 1 CARTON (62756-016-40)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "62756-016-40", "marketing_start_date": "20130617"}], "brand_name": "Testosterone Cypionate", "product_id": "62756-016_bf24bb84-d12f-44e7-98bd-46f3aa792bcc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Androgen Receptor Agonists [MoA]", "Androgen [EPC]", "Androstanes [CS]"], "product_ndc": "62756-016", "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"}