NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4530Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4530Add 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
70518-4530-07051845300030 TABLET in 1 BOTTLE, PLASTIC (70518-4530-0)Marketed from Dec 2, 2025
70518-4530-17051845300190 TABLET in 1 BOTTLE, PLASTIC (70518-4530-1)Marketed from Jan 20, 2026

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 209102
Marketing start
Listing expires
Other FDA classes
GABA A Agonists (Mechanism)GABA B Agonists (Mechanism)
Identifiers
Product ID 70518-4530_5b990755-3981-af68-e063-6294a90aa022SPL ID 5b990755-3981-af68-e063-6294a90aa022
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

N470518453000 followed by a unit qualifier and the quantity

Package 70518-4530-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 209102

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

FDA NDC Directory listings under ANDA 209102
ProductStrengthForm · routeLabelerProduct NDC
BaclofenBaclofen 10 mg/1TabletOralAdvagen Pharma Limited72888-010
BaclofenBaclofen 20 mg/1TabletOralAdvagen Pharma Limited72888-011
BaclofenBaclofen 20 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-312
BaclofenBaclofen 20 mg/1TabletOralBryant Ranch Prepack71335-0949
BaclofenBaclofen 5 mg/1TabletOralAdvagen Pharma Limited72888-009
BaclofenBaclofen 20 mg/1TabletOralREMEDYREPACK INC.70518-4290
BaclofenBaclofen 15 mg/1TabletOralAsclemed USA, Inc.76420-358
BaclofenBaclofen 5 mg/1TabletOralAsclemed USA, Inc.76420-356
BaclofenBaclofen 20 mg/1TabletOralDirect_Rx72189-504
BaclofenBaclofen 10 mg/1TabletOralAsclemed USA, Inc.76420-357
BaclofenBaclofen 20 mg/1TabletOralAsclemed USA, Inc.76420-359
BaclofenBaclofen 5 mg/1TabletOralProficient Rx LP82804-219
BaclofenBaclofen 5 mg/1TabletOralTruPharma LLC52817-319
BaclofenBaclofen 15 mg/1TabletOralTruPharma LLC52817-318
BaclofenBaclofen 10 mg/1TabletOralTruPharma LLC52817-320
BaclofenBaclofen 10 mg/1TabletOralBryant Ranch Prepack71335-9638
BaclofenBaclofen 20 mg/1TabletOralTruPharma LLC52817-321
BaclofenBaclofen 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0568
BaclofenBaclofen 10 mg/1TabletOralProficient Rx LP82804-242
BaclofenBaclofen 10 mg/1TabletOralSOLA Pharmaceuticals, LLC70512-782

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