NDC codes

FDA NDC Directory
Product NDC (as listed)68084-021Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68084-0021Add 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
68084-021-216808400212130 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-021-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-021-11)Marketed from Feb 4, 2013

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)
Abacavir
Generic name (nonproprietary)
abacavir
Active ingredients
Abacavir sulfate — 300 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077844
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A1 Inhibitors (Mechanism)Nucleoside Reverse Transcriptase Inhibitors (Mechanism)
Identifiers
Product ID 68084-021_1ea3a366-c7c0-2e89-e063-6294a90a2419SPL ID 1ea3a366-c7c0-2e89-e063-6294a90a2419SPL set ID 01e46f58-8bda-4ff3-ab21-57d5b540d440RxCUI 242679UNII J220T4J9Q2
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

N468084002121 followed by a unit qualifier and the quantity

Package 68084-0021-21. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Abacavir tablets, in combination with other antiretroviral agents, are indicated for the treatment of human immunodeficiency virus (HIV-1) infection. Abacavir tablets, a nucleoside analogue human immunodeficiency virus (HIV-1) reverse transcriptase inhibitor, are indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077844

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

FDA NDC Directory listings under ANDA 077844
ProductStrengthForm · routeLabelerProduct NDC
AbacavirAbacavir sulfate 300 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-073
AbacavirAbacavir sulfate 300 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6874

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