What is NDC 44911-0317?

44911-0317 is the product NDC for Cerebrapar, Baptisia tinctoria root 3 [hp_X]/mL + 8 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?

Cerebrapar (Baptisia Tinctoria, Cerebrum Suis, Secale Cornutum, Baryta Carbonica, Calcarea Carbonica, Gelsemium Sempervirens, Kali Phosphoricum, Lycopodium Clavatum, Staphysagria).

What is the active ingredient?

Baptisia tinctoria root, Sus scrofa cerebrum, Claviceps purpurea sclerotium, Barium carbonate, Oyster shell calcium carbonate, Crude, Gelsemium sempervirens root, Potassium phosphate, Dibasic, Lycopodium clavatum spore, Delphinium staphisagria seed.

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 Cerebrapar?

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.

Cerebrapar NDC 44911-0317 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0317Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0317Add 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
44911-0317-1	4491103170144911031701	30 mL in 1 BOTTLE, DROPPER (44911-0317-1)Marketed from Jan 11, 2016

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): Cerebrapar
Generic name (nonproprietary): baptisia tinctoria, cerebrum suis, secale cornutum, baryta carbonica, calcarea carbonica, gelsemium sempervirens, kali phosphoricum, lycopodium clavatum, staphysagria
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLSus scrofa cerebrum — 6 [hp_X]/mLClaviceps purpurea sclerotium — 6 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLPotassium phosphate, Dibasic — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLDelphinium staphisagria seed — 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: Jan 11, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0317_c63dccf3-5bbf-4a26-885f-f9c3de29cf4cSPL ID c63dccf3-5bbf-4a26-885f-f9c3de29cf4cSPL set ID cf6b59ee-64dc-4126-ade9-a92b4c7a3af9UNII 5EF0HWI5WU, 4GB5DQR532, 01G9XEA93N, 6P669D8HQ8, 2E32821G6I, 639KR60Q1Q, CI71S98N1Z, C88X29Y479, 00543AP1JVUPC 0363113700541

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

N444911031701 followed by a unit qualifier and the quantity

Package 44911-0317-01. 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 Oct 24, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve nervous twitch, confusion and forgetfulness.** **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 44911-0317

What is NDC 44911-0317?: 44911-0317 is the product NDC for Cerebrapar, Baptisia tinctoria root 3 [hp_X]/mL + 8 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?: Cerebrapar (Baptisia Tinctoria, Cerebrum Suis, Secale Cornutum, Baryta Carbonica, Calcarea Carbonica, Gelsemium Sempervirens, Kali Phosphoricum, Lycopodium Clavatum, Staphysagria).
What is the active ingredient?: Baptisia tinctoria root, Sus scrofa cerebrum, Claviceps purpurea sclerotium, Barium carbonate, Oyster shell calcium carbonate, Crude, Gelsemium sempervirens root, Potassium phosphate, Dibasic, Lycopodium clavatum spore, Delphinium staphisagria seed.
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 Cerebrapar?: 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.