NDC codes

FDA NDC Directory
Product NDC (as listed)0904-7155Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00904-7155Add 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
0904-7155-040090471550430 BLISTER PACK in 1 CARTON (0904-7155-04) / 1 TABLET in 1 BLISTER PACKMarketed from Oct 8, 2009

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)
Buprenorphine
Generic name (nonproprietary)
buprenorphine
Active ingredients
Buprenorphine hydrochloride — 8 mg/1
Dosage form
Tablet
Route
Sublingual
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078633
Marketing start
Listing expires
DEA schedule
CIII
Other FDA classes
Partial Opioid Agonists (Mechanism)
Identifiers
Product ID 0904-7155_b3dcd775-1c37-4433-b66b-744f472c9117SPL ID b3dcd775-1c37-4433-b66b-744f472c9117SPL set ID dba586f9-e3f2-4b9c-849b-907c81a5a0efRxCUI 351264, 351265UNII 56W8MW3EN1
Pharmacologic class
Partial Opioid Agonist

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400904715504 followed by a unit qualifier and the quantity

Package 00904-7155-04. 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)

Buprenorphine Sublingual Tablets are indicated for the treatment of opioid dependence and are preferred for induction. Buprenorphine Sublingual Tablets should be used as part of a complete treatment plan to include counseling and psychosocial support. Buprenorphine Sublingual Tablets contain buprenorphine, a partial opioid agonist, and is indicated for the treatment of opioid dependence and is preferred for induction. ( 1 ) Buprenorphine Sublingual Tablets should be used as part of a complete treatment plan that includes counseling and psychosocial support. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078633

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

FDA NDC Directory listings under ANDA 078633
ProductStrengthForm · routeLabelerProduct NDC
Buprenorphine HClBuprenorphine hydrochloride 2 mg/1TabletSublingualRedpharm Drug67296-2123
Buprenorphine HClBuprenorphine hydrochloride 8 mg/1TabletSublingualREMEDYREPACK INC.70518-2014
Buprenorphine HClBuprenorphine hydrochloride 2 mg/1TabletSublingualREMEDYREPACK INC.70518-2226
Buprenorphine HClBuprenorphine hydrochloride 2 mg/1TabletSublingualClinical Solutions Wholesale, LLC58118-0176
Buprenorphine HClBuprenorphine hydrochloride 8 mg/1TabletSublingualClinical Solutions Wholesale, LLC58118-0177
BuprenorphineBuprenorphine hydrochloride 2 mg/1TabletSublingualHikma Pharmaceuticals USA Inc.0054-0176
Buprenorphine HClBuprenorphine hydrochloride 8 mg/1TabletSublingualBryant Ranch Prepack71335-1163
Buprenorphine Sublingual C-IIIBuprenorphine hydrochloride 2 mg/1TabletSublingualDirect_Rx72189-580
Buprenorphine Sublingual C-IIIBuprenorphine hydrochloride 8 mg/1TabletSublingualDirect_Rx72189-582
BuprenorphineBuprenorphine hydrochloride 2 mg/1TabletSublingualMajor Pharmaceuticals0904-7154
BuprenorphineBuprenorphine hydrochloride 8 mg/1TabletSublingualHikma Pharmaceuticals USA Inc.0054-0177

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