United States · FDA National Drug Code directory
Endopar F
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
- 44911-0308_87d22a70-0356-477c-9085-9a7d351bbfc8
- Product NDC
- 44911-0308
- Form
- LIQUID
- Composition / generic term
- Cimicifuga Racemosa, Fucus Vesiculosus, Oophorinum (Suis), Hypophysis Suis, Thyroidinum (Suis), Graphites, Lachesis Mutus, Natrum Muriaticum, Pulsatilla (Pratensis), Sepia
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20151130
- Source listing expiry
- 20261231
Source-listed ingredients
- BLACK COHOSH — 3 [hp_X]/mL
- FUCUS VESICULOSUS — 3 [hp_X]/mL
- SUS SCROFA OVARY — 6 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND — 6 [hp_X]/mL
- THYROID — 6 [hp_X]/mL
- GRAPHITE — 12 [hp_X]/mL
- LACHESIS MUTA VENOM — 12 [hp_X]/mL
- SODIUM CHLORIDE — 12 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE — 12 [hp_X]/mL
- SEPIA OFFICINALIS JUICE — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (44911-0308-1) · 44911-0308-1
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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