NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2669Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2669Add 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
71335-2669-17133526690171335266901100 TABLET in 1 BOTTLE (71335-2669-1)Marketed from Jun 26, 2025
71335-2669-271335266902713352669021000 TABLET in 1 BOTTLE (71335-2669-2)Marketed from Jun 26, 2025
71335-2669-37133526690371335266903120 TABLET in 1 BOTTLE (71335-2669-3)Marketed from Jun 26, 2025

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)
Baclofen
Generic name (nonproprietary)
baclofen
Active ingredients
Baclofen — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212378
Marketing start
Listing expires
Other FDA classes
GABA A Agonists (Mechanism)GABA B Agonists (Mechanism)
Identifiers
Product ID 71335-2669_21d9a176-5277-4fa4-83c5-91ef3743368dSPL ID 21d9a176-5277-4fa4-83c5-91ef3743368dSPL set ID 3ac0f0d2-86d8-46d0-88e5-c243734b0814RxCUI 197392UNII H789N3FKE8
Pharmacologic class
gamma-Aminobutyric Acid-ergic 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335266901 followed by a unit qualifier and the quantity

Package 71335-2669-01. 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.

About NDC 71335-2669

What is NDC 71335-2669?
71335-2669 is the product NDC for Baclofen, Baclofen 20 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Baclofen.
What is the active ingredient?
Baclofen.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Baclofen?
219 other product NDCs are listed under this name. See all Baclofen 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 Baclofen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BaclofenBaclofen 10 mg/5mLSolutionOralAcella Pharmaceuticals, LLC42192-63142192-0631-4042192-0631-45
BaclofenBaclofen 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-416268788-4162-0168788-4162-0368788-4162-06+2 more
BaclofenBaclofen 5 mg/1TabletOralREMEDYREPACK INC.70518-465670518-4656-00
BaclofenBaclofen 10 mg/1TabletOralCoupler LLC67046-107267046-1072-03
BaclofenBaclofen 20 mg/1TabletOralMedcore LLC82461-71882461-0718-10
BaclofenBaclofen 10 mg/1TabletOralMedcore LLC82461-71782461-0717-10
BaclofenBaclofen 10 mg/1TabletOralCardinal Health 107, LLC55154-019855154-0198-00
BaclofenBaclofen 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-056880425-0568-0180425-0568-0280425-0568-03+1 more
BaclofenBaclofen 20 mg/1TabletOralREMEDYREPACK INC.70518-453070518-4530-0070518-4530-01
BaclofenBaclofen 5 mg/1TabletOralAurobindo Pharma Limited84386-03584386-0035-01

All 220 Baclofen NDCs

Other NDCs under ANDA 212378

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

FDA NDC Directory listings under ANDA 212378
ProductStrengthForm · routeLabelerProduct NDC
BaclofenBaclofen 10 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0156
BaclofenBaclofen 5 mg/1TabletOralBryant Ranch Prepack72162-2372
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack72162-2373
BaclofenBaclofen 20 mg/1TabletOralBryant Ranch Prepack72162-2374
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack71335-2826
BaclofenBaclofen 10 mg/1TabletOralREMEDYREPACK INC.70518-3089
BaclofenBaclofen 20 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0205
BaclofenBaclofen 20 mg/1TabletOralREMEDYREPACK INC.70518-3115
BaclofenBaclofen 5 mg/1TabletOralMethod Pharmaceuticals LLC58657-730
BaclofenBaclofen 10 mg/1TabletOralMethod Pharmaceuticals LLC58657-731
BaclofenBaclofen 20 mg/1TabletOralMethod Pharmaceuticals LLC58657-732
BaclofenBaclofen 20 mg/1TabletOralBryant Ranch Prepack71335-1796
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack71335-1797
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack63629-1224
BaclofenBaclofen 5 mg/1TabletOralMethod Pharmaceuticals LLC58657-930
BaclofenBaclofen 10 mg/1TabletOralMethod Pharmaceuticals LLC58657-931
BaclofenBaclofen 20 mg/1TabletOralMethod Pharmaceuticals LLC58657-932
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack63629-1225
BaclofenBaclofen 20 mg/1TabletOralXLCare Pharmaceuticals Inc.72865-298
BaclofenBaclofen 5 mg/1TabletOralXLCare Pharmaceuticals Inc.72865-296

Showing 20 of 29.

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