What is NDC 44911-0308?

44911-0308 is the product NDC for Endopar F, Black cohosh 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Endopar F (Cimicifuga Racemosa, Fucus Vesiculosus, Oophorinum (Suis), Hypophysis Suis, Thyroidinum (Suis), Graphites, Lachesis Mutus, Natrum Muriaticum, Pulsatilla (Pratensis), Sepia).

What is the active ingredient?

Black cohosh, Fucus vesiculosus, Sus scrofa ovary, Sus scrofa pituitary gland, Thyroid, Graphite, Lachesis muta venom, Sodium chloride, Pulsatilla pratensis whole, Sepia officinalis juice.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Endopar F?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Endopar F NDC 44911-0308 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0308Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0308Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0308-1	4491103080144911030801	30 mL in 1 BOTTLE, DROPPER (44911-0308-1)Marketed from Nov 30, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Endopar FSuffix: F
Generic name (nonproprietary): cimicifuga racemosa, fucus vesiculosus, oophorinum (suis), hypophysis suis, thyroidinum (suis), graphites, lachesis mutus, natrum muriaticum, pulsatilla (pratensis), sepia
Active ingredients: Black cohosh — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLSus scrofa ovary — 6 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLGraphite — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 30, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0308_87d22a70-0356-477c-9085-9a7d351bbfc8SPL ID 87d22a70-0356-477c-9085-9a7d351bbfc8SPL set ID d186ae0e-0dc3-48e7-9e22-6778bb80ad18UNII K73E24S6X9, 535G2ABX9M, S7YTV04R8O, L0PFEMQ1DT, 6RV024OAUQ, 4QQN74LH4O, VSW71SS07I, 451W47IQ8X, 8E272251DI, QDL83WN8C2

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911030801 followed by a unit qualifier and the quantity

Package 44911-0308-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jun 7, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve menstrual pain and cramps, pain immediately prior to menses, and sore breasts associated with menstruation.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 44911-0308

What is NDC 44911-0308?: 44911-0308 is the product NDC for Endopar F, Black cohosh 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Endopar F (Cimicifuga Racemosa, Fucus Vesiculosus, Oophorinum (Suis), Hypophysis Suis, Thyroidinum (Suis), Graphites, Lachesis Mutus, Natrum Muriaticum, Pulsatilla (Pratensis), Sepia).
What is the active ingredient?: Black cohosh, Fucus vesiculosus, Sus scrofa ovary, Sus scrofa pituitary gland, Thyroid, Graphite, Lachesis muta venom, Sodium chloride, Pulsatilla pratensis whole, Sepia officinalis juice.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Endopar F?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.