NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9681Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9681Add 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
71335-9681-071335968100120 TABLET in 1 BOTTLE, PLASTIC (71335-9681-0)Marketed from Dec 12, 2024
71335-9681-17133596810190 TABLET in 1 BOTTLE, PLASTIC (71335-9681-1)Marketed from Dec 12, 2024
71335-9681-27133596810220 TABLET in 1 BOTTLE, PLASTIC (71335-9681-2)Marketed from Dec 12, 2024
71335-9681-37133596810360 TABLET in 1 BOTTLE, PLASTIC (71335-9681-3)Marketed from Dec 12, 2024
71335-9681-47133596810445 TABLET in 1 BOTTLE, PLASTIC (71335-9681-4)Marketed from Dec 12, 2024
71335-9681-571335968105112 TABLET in 1 BOTTLE, PLASTIC (71335-9681-5)Marketed from Dec 12, 2024
71335-9681-67133596810630 TABLET in 1 BOTTLE, PLASTIC (71335-9681-6)Marketed from Dec 12, 2024
71335-9681-77133596810756 TABLET in 1 BOTTLE, PLASTIC (71335-9681-7)Marketed from Dec 12, 2024
71335-9681-87133596810815 TABLET in 1 BOTTLE, PLASTIC (71335-9681-8)Marketed from Dec 12, 2024
71335-9681-97133596810984 TABLET in 1 BOTTLE, PLASTIC (71335-9681-9)Marketed from Dec 12, 2024

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077068
Marketing start
Listing expires
Other FDA classes
GABA A Agonists (Mechanism)GABA B Agonists (Mechanism)
Identifiers
Product ID 71335-9681_b63760e4-d4d2-47a9-ac83-a08352a16435SPL ID b63760e4-d4d2-47a9-ac83-a08352a16435SPL set ID 7b6d33d8-58c2-448d-a8df-1de7339b1520RxCUI 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

N471335968100 followed by a unit qualifier and the quantity

Package 71335-9681-00. 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)

INDICATIONS AND USAGE Baclofen tablets USP are useful for the alleviation of signs and symptoms of spasticity resulting from multiple sclerosis, particularly for the relief of flexor spasms and concomitant pain, clonus, and muscular rigidity. Patients should have reversible spasticity so that baclofen treatment will aid in restoring residual function. Baclofen tablets USP may also be of some value in patients with spinal cord injuries and other spinal cord diseases. Baclofen tablets USP are not indicated in the treatment of skeletal muscle spasm resulting from rheumatic disorders. The efficacy of baclofen in stroke, cerebral palsy, and Parkinson’s disease has not been established and, theref…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077068

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

FDA NDC Directory listings under ANDA 077068
ProductStrengthForm · routeLabelerProduct NDC
BaclofenBaclofen 10 mg/1TabletOralPar Health USA, LLC0603-2406
BaclofenBaclofen 20 mg/1TabletOralPar Health USA, LLC0603-2407
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack63629-2128
BaclofenBaclofen 20 mg/1TabletOralBryant Ranch Prepack63629-2130
BaclofenBaclofen 20 mg/1TabletOralBryant Ranch Prepack63629-2131

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