United States · FDA National Drug Code directory
My Choice TM
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
- 62756-720_8f45ff33-3872-495f-a05d-e74e0b4dc0c4
- Product NDC
- 62756-720
- Form
- TABLET
- Composition / generic term
- levonorgestrel
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180401
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVONORGESTREL — 1.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (62756-720-60) / 1 TABLET in 1 BLISTER PACK · 62756-720-60
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →