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: 76420-580_3485f152-22bd-e5bd-e063-6394a90afa5b
Product NDC: 76420-580
Form: CAPSULE
Composition / generic term: PROGESTERONE
Labeler: Asclemed USA, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20181128
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 (76420-580-10) · 76420-580-10
30 CAPSULE in 1 BOTTLE (76420-580-30) · 76420-580-30
60 CAPSULE in 1 BOTTLE (76420-580-60) · 76420-580-60
90 CAPSULE in 1 BOTTLE (76420-580-90) · 76420-580-90

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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