NDC codes

FDA NDC Directory
Product NDC (as listed)72189-690Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0690Add 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
72189-690-907218906909090 TABLET, FILM COATED in 1 BOTTLE (72189-690-90)Marketed from Sep 23, 2026

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)
Carvedilol
Generic name (nonproprietary)
carvedilol
Active ingredients
Carvedilol — 12.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Direct_RxNDC labeler code 72189
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077614
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers
Product ID 72189-690_5c297a25-6195-45c1-e063-6294a90ae8edSPL ID 5c297a25-6195-45c1-e063-6294a90ae8ed
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

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

N472189069090 followed by a unit qualifier and the quantity

Package 72189-0690-90. 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 72189-690

What is NDC 72189-690?
72189-690 is the product NDC for Carvedilol, Carvedilol 12.5 mg/1 tablet, film coated, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Carvedilol.
What is the active ingredient?
Carvedilol.
Who is the labeler?
Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Carvedilol?
168 other product NDCs are listed under this name. See all Carvedilol 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 Carvedilol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralCoupler LLC67046-097367046-0973-03
CarvedilolCarvedilol 12.5 mg/1Tablet, Film coatedOralCoupler LLC67046-087967046-0879-03
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralCoupler LLC67046-033667046-0336-03
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralDirect_Rx72189-66472189-0664-60
CarvedilolCarvedilol 25 mg/1Tablet, Film coatedOralDirect_Rx72189-66372189-0663-90
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralDirect_Rx72189-65372189-0653-90
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralCoupler LLC67046-161667046-1616-03
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-49972888-0499-0172888-0499-0272888-0499-03
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-50072888-0500-0172888-0500-0272888-0500-03
CarvedilolCarvedilol 12.5 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-50172888-0501-0172888-0501-0272888-0501-03

All 169 Carvedilol NDCs

Other NDCs under ANDA 077614

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

FDA NDC Directory listings under ANDA 077614
ProductStrengthForm · routeLabelerProduct NDC
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralQPharma Inc42708-181
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1062
CarvedilolCarvedilol 12.5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1067
CarvedilolCarvedilol 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4171
CarvedilolCarvedilol 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5726
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6742
CarvedilolCarvedilol 12.5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6878
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6949
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7786
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-029
CarvedilolCarvedilol 12.5 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-030
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-034
CarvedilolCarvedilol 25 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-397
CarvedilolCarvedilol 12.5 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-494
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-582
CarvedilolCarvedilol 6.25 mg/1Tablet, Film coatedOralProficient Rx LP63187-424
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralProficient Rx LP63187-570
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-4060
CarvedilolCarvedilol 25 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-4070
CarvedilolCarvedilol 3.125 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-616

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