United States · FDA National Drug Code directory
Estradiol and Norethindrone Acetate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50742-657_b156b1fa-c3f8-42fd-a8e3-e1f9c58e0175
- Product NDC
- 50742-657
- Form
- TABLET
- Composition / generic term
- Estradiol and Norethindrone Acetate
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190403
- Source listing expiry
- 20271231
Source-listed ingredients
- ESTRADIOL — 1 mg/1
- NORETHINDRONE ACETATE — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (50742-657-28) / 28 TABLET in 1 BLISTER PACK · 50742-657-28
- 6 BLISTER PACK in 1 CARTON (50742-657-68) / 28 TABLET in 1 BLISTER PACK · 50742-657-68
- 3 BLISTER PACK in 1 CARTON (50742-657-84) / 28 TABLET in 1 BLISTER PACK · 50742-657-84
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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