NDC codes

FDA NDC Directory
Product NDC (as listed)0074-9036Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00074-9036Add 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 NDC11-digit (billing)PackageCopy
0074-9036-300007490363030 CAPSULE, LIQUID FILLED in 1 BOTTLE (0074-9036-30)Marketed from Apr 20, 2018

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Zemplar
Generic name (nonproprietary)
paricalcitol
Active ingredients
Paricalcitol — 1 ug/1
Dosage form
Capsule, Liquid filled
Route
Oral
Labeler
AbbVie Inc.NDC labeler code 0074
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021606
Marketing start
Marketing end
Other FDA classes
Ergocalciferols (Chemical structure)
Identifiers
Product ID 0074-9036_61ef39c0-0c32-4b82-962e-8ebdd55ce427SPL ID 61ef39c0-0c32-4b82-962e-8ebdd55ce427SPL set ID 1b27c026-2d60-47b4-2a9c-ded1818f21b5RxCUI 577315, 577317, 606854, 606859UNII 6702D36OG5UPC 0300749036309, 0300749037306
Pharmacologic class
Vitamin D Analog; Vitamin D2 Analog

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

N400074903630 followed by a unit qualifier and the quantity

Package 00074-9036-30. 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 .

Indications (excerpt from the label)

ZEMPLAR is a vitamin D analog indicated in adults and pediatric patients 10 years and older for the prevention and treatment of secondary hyperparathyroidism associated with: Chronic kidney disease (CKD) Stages 3 and 4 ( 1.1 ). CKD Stage 5 in patients on hemodialysis or peritoneal dialysis ( 1.2 ). 1.1 Chronic Kidney Disease Stages 3 and 4 ZEMPLAR capsules are indicated in adults and pediatric patients 10 years of age and older for the prevention and treatment of secondary hyperparathyroidism associated with Chronic Kidney Disease (CKD) Stages 3 and 4. 1.2 Chronic Kidney Disease Stage 5 ZEMPLAR capsules are indicated in adults and pediatric patients 10 years of age and older for the preventi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0074-9036

What is NDC 0074-9036?
0074-9036 is the product NDC for Zemplar (paricalcitol), Paricalcitol 1 ug/1 capsule, liquid filled, listed with the FDA by AbbVie Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Zemplar (Paricalcitol).
What is the active ingredient?
Paricalcitol.
Who is the labeler?
AbbVie Inc., NDC labeler code 0074. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Zemplar?
3 other product NDCs are listed under this name. See all Zemplar NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Zemplar NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ZemplarparicalcitolParicalcitol 2 ug/1Capsule, Liquid filledOralAbbVie Inc.0074-903700074-9037-30
ZemplarparicalcitolParicalcitol 5 ug/mLInjection, SolutionIntravenousAbbVie Inc.0074-165800074-1658-0100074-1658-05
ZemplarparicalcitolParicalcitol 2 ug/mLInjection, SolutionIntravenousAbbVie Inc.0074-463700074-4637-01

Other NDCs under NDA 021606

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 021606
ProductStrengthForm · routeLabelerProduct NDC
ZemplarparicalcitolParicalcitol 2 ug/1Capsule, Liquid filledOralAbbVie Inc.0074-9037

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