United States · FDA National Drug Code directory
Progesterone
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
- 76420-282_e8bb17c7-a664-6cfb-e053-2995a90af31f
- Product NDC
- 76420-282
- Form
- CAPSULE
- Composition / generic term
- Progesterone
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210108
- Source listing expiry
- 20261231
Source-listed ingredients
- PROGESTERONE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (76420-282-01) · 76420-282-01
- 30 CAPSULE in 1 BOTTLE (76420-282-30) · 76420-282-30
- 60 CAPSULE in 1 BOTTLE (76420-282-60) · 76420-282-60
- 90 CAPSULE in 1 BOTTLE (76420-282-90) · 76420-282-90
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 →