What is NDC 44911-0212?

44911-0212 is the product NDC for Parathyroid Cord (parathyroid gland (suis)), Sus scrofa parathyroid gland 12 [hp_X]/mL 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?

Parathyroid Cord (Parathyroid gland (suis)).

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 Parathyroid Cord?

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.

Parathyroid Cord NDC 44911-0212 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0212Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0212Add 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
44911-0212-1	4491102120144911021201	30 mL in 1 BOTTLE, DROPPER (44911-0212-1)Marketed from Jul 16, 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): Parathyroid Cord
Generic name (nonproprietary): parathyroid gland (suis)
Active ingredients: Sus scrofa parathyroid gland — 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: Jul 16, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0212_9d1fab43-e3a2-4340-9387-96c7b81a509cSPL ID 9d1fab43-e3a2-4340-9387-96c7b81a509cSPL set ID 26cef977-2756-43f6-91e7-7b3995acd461UNII 2KBE35NE8SUPC 0363113600261

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

N444911021201 followed by a unit qualifier and the quantity

Package 44911-0212-01. 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 29, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve bone and muscle issues.** **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 44911-0212

What is NDC 44911-0212?: 44911-0212 is the product NDC for Parathyroid Cord (parathyroid gland (suis)), Sus scrofa parathyroid gland 12 [hp_X]/mL 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?: Parathyroid Cord (Parathyroid gland (suis)).
What is the active ingredient?: Sus scrofa parathyroid gland.
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 Parathyroid Cord?: 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.

Parathyroid Cord (Parathyroid gland (suis)) NDC 44911-0212