NDC codes

FDA NDC Directory
Product NDC (as listed)49702-211Labeler and product segments. Claims need a package NDC.
Product NDC at billing width49702-0211Add 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
49702-211-204970202112049702021120100 CAPSULE in 1 BOTTLE (49702-211-20)Marketed from Oct 28, 2010

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Retrovir
Generic name (nonproprietary)
zidovudine
Active ingredients
Zidovudine — 100 mg/1
Dosage form
Capsule
Route
Oral
Labeler
ViiV Healthcare CompanyNDC labeler code 49702
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 019655
Marketing start
Listing expires
Other FDA classes
Nucleoside Reverse Transcriptase Inhibitors (Mechanism)
Identifiers
Product ID 49702-211_175380c2-4c45-4f26-88db-9154a47cf795SPL ID 175380c2-4c45-4f26-88db-9154a47cf795
Pharmacologic class
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor

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

N449702021120 followed by a unit qualifier and the quantity

Package 49702-0211-20. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 49702-211

What is NDC 49702-211?
49702-211 is the product NDC for Retrovir (zidovudine), Zidovudine 100 mg/1 capsule, listed with the FDA by ViiV Healthcare Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Retrovir (Zidovudine).
What is the active ingredient?
Zidovudine.
Who is the labeler?
ViiV Healthcare Company, NDC labeler code 49702. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Retrovir?
2 other product NDCs are listed under this name. See all Retrovir 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 Retrovir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
RetrovirzidovudineZidovudine 10 mg/mLInjection, SolutionIntravenousViiV Healthcare Company49702-21349702-0213-26
RetrovirzidovudineZidovudine 10 mg/mLSolutionOralViiV Healthcare Company49702-21249702-0212-48

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