51991-474 : Estradiol / Norethindrone Acetate (Estradiol 1 mg / Norethindrone Acetate 0.5 mg)


NDC: 51991-474
Labeler: Breckenridge Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Drug Name:  Estradiol / Norethindrone Acetate
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA078324
Rev. Date: 


Appearance:


Markings: B;474
Shapes:  Round
Colors:  White
Size (mm): 6
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 51991-474-28: 1 BLISTER PACK IN 1 CARTON (51991‑474‑28) > 28 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Estradiol
  • Norethindrone Acetate

Dosage Strength:

  • 1 mg
  • .5 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Starch, Corn
  • Copovidone
  • Talc
  • Magnesium Stearate
  • Hypromelloses
  • Triacetin

Pharmaceutical Classes:

  • Estradiol Congeners [Chemical/Ingredient]
  • Estrogen [EPC]
  • Estrogen Receptor Agonists [MoA]
  • Progesterone Congeners [Chemical/Ingredient]
  • Progestin [EPC]

Related Products:

Based on records with the same trade name.
  • 51991-623 Estradiol / Norethindrone Acetate (Estradiol 0.5 mg / Norethindrone Acetate 0.1 mg) by Breckenridge Pharmaceutical, Inc.
  • 54868-4677 Estradiol / Norethindrone Acetate (Estradiol 1 mg / Norethindrone Acetate 0.5 mg) by Physicians Total Care, Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.