medroxyprogesterone acetate

Generic: medroxyprogesterone acetate

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

Drug Facts

Product Profile

Brand Name medroxyprogesterone acetate
Generic Name medroxyprogesterone acetate
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, SUSPENSION
Routes
INTRAMUSCULAR
Active Ingredients

medroxyprogesterone acetate 150 mg/mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-090
Product ID 62756-090_8e776908-1e91-4e7e-b3c1-e6fe8234ba75
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210760
Listing Expiration 2026-12-31
Marketing Start 2019-05-04

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756090
Hyphenated Format 62756-090

Supplemental Identifiers

RxCUI
1000126
UNII
C2QI4IOI2G

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 medroxyprogesterone acetate (source: ndc)
Generic Name medroxyprogesterone acetate (source: ndc)
Application Number ANDA210760 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 150 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (62756-090-40) / 1 mL in 1 VIAL, SINGLE-DOSE
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (62756-090-45) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

Ingredients (1)

medroxyprogesterone acetate (150 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "8e776908-1e91-4e7e-b3c1-e6fe8234ba75", "openfda": {"unii": ["C2QI4IOI2G"], "rxcui": ["1000126"], "spl_set_id": ["d1ea4098-6196-421f-b8e1-bcb31a061e04"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (62756-090-40)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "62756-090-40", "marketing_start_date": "20190504"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (62756-090-45)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "62756-090-45", "marketing_start_date": "20190504"}], "brand_name": "MEDROXYPROGESTERONE ACETATE", "product_id": "62756-090_8e776908-1e91-4e7e-b3c1-e6fe8234ba75", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "62756-090", "generic_name": "MEDROXYPROGESTERONE ACETATE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEDROXYPROGESTERONE ACETATE", "active_ingredients": [{"name": "MEDROXYPROGESTERONE ACETATE", "strength": "150 mg/mL"}], "application_number": "ANDA210760", "marketing_category": "ANDA", "marketing_start_date": "20190504", "listing_expiration_date": "20261231"}