NDC codes

FDA NDC Directory
Product NDC (as listed)63629-8717Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-8717Add 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
63629-8717-16362987170130 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-8717-1)Marketed from Oct 24, 2011

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)
Olanzapine
Generic name (nonproprietary)
olanzapine
Active ingredients
Olanzapine — 5 mg/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091265
Marketing start
Listing expires
Identifiers
Product ID 63629-8717_3363cea7-b182-09e6-e063-6294a90ae027SPL ID 3363cea7-b182-09e6-e063-6294a90ae027SPL set ID d3857220-d9ff-4820-bf53-f2384b59a1a6RxCUI 314155UNII N7U69T4SZR
Pharmacologic class
Atypical Antipsychotic

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

N463629871701 followed by a unit qualifier and the quantity

Package 63629-8717-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 091265

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

FDA NDC Directory listings under ANDA 091265
ProductStrengthForm · routeLabelerProduct NDC
OlanzapineOlanzapine 10 mg/1Tablet, Orally disintegratingOralApotex Corp.60505-3276
OlanzapineOlanzapine 5 mg/1Tablet, Orally disintegratingOralApotex Corp.60505-3275
OlanzapineOlanzapine 15 mg/1Tablet, Orally disintegratingOralApotex Corp.60505-3277
OlanzapineOlanzapine 20 mg/1Tablet, Orally disintegratingOralApotex Corp.60505-3278
OlanzapineOlanzapine 10 mg/1Tablet, Orally disintegratingOralGolden State Medical Supply, Inc.51407-262
OlanzapineOlanzapine 5 mg/1Tablet, Orally disintegratingOralGolden State Medical Supply, Inc.51407-261
OlanzapineOlanzapine 15 mg/1Tablet, Orally disintegratingOralGolden State Medical Supply, Inc.51407-263
OlanzapineOlanzapine 20 mg/1Tablet, Orally disintegratingOralGolden State Medical Supply, Inc.51407-264
OlanzapineOlanzapine 5 mg/1Tablet, Orally disintegratingOralCoupler LLC67046-1550
OlanzapineOlanzapine 10 mg/1Tablet, Orally disintegratingOralCoupler LLC67046-1565
OlanzapineOlanzapine 15 mg/1Tablet, Orally disintegratingOralBryant Ranch Prepack63629-8714
OlanzapineOlanzapine 10 mg/1Tablet, Orally disintegratingOralBryant Ranch Prepack63629-8718

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