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
- 71335-2242_c9c8915b-47cc-4b82-b222-d664d5f3e739
- Product NDC
- 71335-2242
- Form
- CAPSULE
- Composition / generic term
- PROGESTERONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181128
- Source listing expiry
- 20271231
Source-listed ingredients
- PROGESTERONE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 CAPSULE in 1 BOTTLE (71335-2242-0) · 71335-2242-0
- 30 CAPSULE in 1 BOTTLE (71335-2242-1) · 71335-2242-1
- 28 CAPSULE in 1 BOTTLE (71335-2242-2) · 71335-2242-2
- 18 CAPSULE in 1 BOTTLE (71335-2242-3) · 71335-2242-3
- 90 CAPSULE in 1 BOTTLE (71335-2242-4) · 71335-2242-4
- 100 CAPSULE in 1 BOTTLE (71335-2242-5) · 71335-2242-5
- 6 CAPSULE in 1 BOTTLE (71335-2242-6) · 71335-2242-6
- 60 CAPSULE in 1 BOTTLE (71335-2242-7) · 71335-2242-7
- 180 CAPSULE in 1 BOTTLE (71335-2242-8) · 71335-2242-8
- 10 CAPSULE in 1 BOTTLE (71335-2242-9) · 71335-2242-9
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 →