Depo-SubQ Provera Product NDC number 0009-4709 (medroxyprogesterone acetate Drug)

Depo-SubQ Provera Product NDC number 0009-4709 (medroxyprogesterone acetate Drug)
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What is Depo-SubQ Provera and Depo-SubQ Provera Product NDC number? Below is the most updated information on the Product NDC number 0009-4709 – Depo-SubQ Provera drug (medroxyprogesterone acetate). Medical Code Data provides all information of this drug products including NDC product code, labeler name, dosage form & certification date.

What is Depo-SubQ Provera?

Depo-SubQ Provera is a HUMAN PRESCRIPTION DRUG labeled by Pharmacia and Upjohn Company LLC. Depo-SubQ Provera, commonly known as medroxyprogesterone acetate, is assigned Product NDC number 0009-4709. Depo-SubQ Provera is marketed under the NDA category with application number NDA021583. Depo-SubQ Provera‘s dosage form is INJECTION, SUSPENSION and is administered via SUBCUTANEOUS form.

General Information

  • Proprietary Name / Trade Name: Depo-SubQ Provera
  • Non Proprietary Name / Generic Name: medroxyprogesterone acetate
  • Proprietary Name Suffix: 

Uses & dosage information

  • Route Name: SUBCUTANEOUS
  • Active strength Number: 104
  • Active Strength Unit: mg/.65mL
  • Pharm Classes: Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

We are updating more information on uses, dosage, side effects, warnings, reviews and pictures of Depo-SubQ Provera (generic name Depo-SubQ Provera) – Product NDC number 0009-4709 . Please visit frequently to get the most updated information

Distribution information

  • Marketing Category Name: NDA
  • Labeler Name: Pharmacia and Upjohn Company LLC
  • NDC Exclude Flag: N
  • FDA Public: Approved (Please Visit FDA for latest update)
  • Product ID: 0009-4709_2219a0ef-8b1c-48f8-947b-3be2798a6314
  • Product NDC Number: 0009-4709
  • Application Number: NDA021583
  • Start Marketing Date: 2005-05-02
  • End Marketing Date:–
  • Listing Record Certified Through: 2018-12-31

Above are up-to-date information of Depo-SubQ Provera – 0009-4709. There are no other drug products that have the same NDC identifier number. You can lookup more NDC number by clicking here

Useful information of the NDC Directory by FDA

What is NDC?

NDC (stands for National Drug Code) is a universal product identifier for human drugs manufactured, prepared, propagated, compounded, or processed for commercial distribution in the United States. An NDC number for a specific drug is created by the the FDA and the manufacturer to ensure that products can be differentiated. The NDC database includes all information submitted to the FDA as part of drug listing requirements under section 510 of the FD&C Act, 21 USC 360.

How is the NDC formatted?

An NDC number contains 3 segments: the labeler code (identifies the manufacturer, repackager or distributor), the product code (identifies a specific strength, dosage form, and formulation) and the package code (identifies package types and sizes).

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Important notes regarding NDC

  • Assignment of an NDC number does not in any way denote FDA approval of the product.
  • Assignment of an NDC number does not denote that a product is covered or eligible for reimbursement by Medicare, Medicaid or other payers.
  • National Drug Code Directory does not include animal drugs, blood products, or human drugs that are not in final marketed form, such as Active Pharmaceutical Ingredients(APIs), drugs for further processing,…

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DISCLAIMER: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.


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