medroxyprogesterone acetate

Generic: medroxyprogesterone acetate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name medroxyprogesterone acetate
Generic Name medroxyprogesterone acetate
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

medroxyprogesterone acetate 5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0555-0873
Product ID 0555-0873_b8f519a9-a8d0-4dd5-b138-564fb579c461
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040159
Listing Expiration 2026-12-31
Marketing Start 1996-12-03

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05550873
Hyphenated Format 0555-0873

Supplemental Identifiers

RxCUI
1000114 1000135 1000141
UPC
0305550873020 0305550872023
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 ANDA040159 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0555-0873-02)
  • 500 TABLET in 1 BOTTLE (0555-0873-04)
source: ndc

Packages (2)

Ingredients (1)

medroxyprogesterone acetate (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b8f519a9-a8d0-4dd5-b138-564fb579c461", "openfda": {"upc": ["0305550873020", "0305550872023"], "unii": ["C2QI4IOI2G"], "rxcui": ["1000114", "1000135", "1000141"], "spl_set_id": ["9eb200b0-db96-4a51-87ea-04db862978c8"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0873-02)", "package_ndc": "0555-0873-02", "marketing_start_date": "19961204"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0555-0873-04)", "package_ndc": "0555-0873-04", "marketing_start_date": "19961204"}], "brand_name": "Medroxyprogesterone Acetate", "product_id": "0555-0873_b8f519a9-a8d0-4dd5-b138-564fb579c461", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0555-0873", "generic_name": "Medroxyprogesterone Acetate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Medroxyprogesterone Acetate", "active_ingredients": [{"name": "MEDROXYPROGESTERONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA040159", "marketing_category": "ANDA", "marketing_start_date": "19961203", "listing_expiration_date": "20261231"}