NDC codes

FDA NDC Directory
Product NDC (as listed)0071-1018Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00071-1018Add 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
0071-1018-680007110186890 CAPSULE in 1 BOTTLE (0071-1018-68)Marketed from Dec 30, 2004

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)
Lyrica
Generic name (nonproprietary)
pregabalin
Active ingredients
Pregabalin — 300 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Parke-Davis Div of Pfizer IncNDC labeler code 0071
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021446
Marketing start
Marketing end
DEA schedule
CV
Identifiers
Product ID 0071-1018_e7c79058-03ba-4e7f-9a31-9ec5ce245161SPL ID e7c79058-03ba-4e7f-9a31-9ec5ce245161SPL set ID 60185c88-ecfd-46f9-adb9-b97c6b00a553RxCUI 483438, 483440, 483442, 483444, 483446, 483448, 483450, 577127, 607018, 607020, 607022, 607024, 607026, 607028, 607033, 607038, 898715, 898718UNII 55JG375S6MUPC 0300711012683

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

N400071101868 followed by a unit qualifier and the quantity

Package 00071-1018-68. 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)

LYRICA is indicated for: • Management of neuropathic pain associated with diabetic peripheral neuropathy • Management of postherpetic neuralgia • Adjunctive therapy for the treatment of partial-onset seizures in patients 1 month of age and older • Management of fibromyalgia • Management of neuropathic pain associated with spinal cord injury LYRICA is indicated for: • Neuropathic pain associated with diabetic peripheral neuropathy (DPN) ( 1 ) • Postherpetic neuralgia (PHN) ( 1 ) • Adjunctive therapy for the treatment of partial-onset seizures in patients 1 month of age and older ( 1 ) • Fibromyalgia ( 1 ) • Neuropathic pain associated with spinal cord injury ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0071-1018

What is NDC 0071-1018?
0071-1018 is the product NDC for Lyrica (pregabalin), Pregabalin 300 mg/1 capsule, listed with the FDA by Parke-Davis Div of Pfizer Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lyrica (Pregabalin).
What is the active ingredient?
Pregabalin.
Who is the labeler?
Parke-Davis Div of Pfizer Inc, NDC labeler code 0071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lyrica?
9 other product NDCs are listed under this name. See all Lyrica 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 Lyrica NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LyricapregabalinPregabalin 300 mg/1CapsuleOralViatris Specialty LLC58151-24258151-0242-77
LyricapregabalinPregabalin 75 mg/1CapsuleOralViatris Specialty LLC58151-23858151-0238-7758151-0238-88
LyricapregabalinPregabalin 200 mg/1CapsuleOralViatris Specialty LLC58151-24158151-0241-77
LyricapregabalinPregabalin 225 mg/1CapsuleOralViatris Specialty LLC58151-24358151-0243-77
LyricapregabalinPregabalin 25 mg/1CapsuleOralViatris Specialty LLC58151-23658151-0236-77
LyricapregabalinPregabalin 50 mg/1CapsuleOralViatris Specialty LLC58151-23758151-0237-7758151-0237-88
LyricapregabalinPregabalin 150 mg/1CapsuleOralViatris Specialty LLC58151-24058151-0240-7758151-0240-88
LyricapregabalinPregabalin 100 mg/1CapsuleOralViatris Specialty LLC58151-23958151-0239-7758151-0239-88
LyricapregabalinPregabalin 20 mg/mLSolutionOralViatris Specialty LLC58151-24458151-0244-35

Other NDCs under NDA 021446

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

FDA NDC Directory listings under NDA 021446
ProductStrengthForm · routeLabelerProduct NDC
LyricapregabalinPregabalin 75 mg/1CapsuleOralViatris Specialty LLC58151-238
LyricapregabalinPregabalin 25 mg/1CapsuleOralViatris Specialty LLC58151-236
LyricapregabalinPregabalin 50 mg/1CapsuleOralViatris Specialty LLC58151-237
LyricapregabalinPregabalin 200 mg/1CapsuleOralViatris Specialty LLC58151-241
LyricapregabalinPregabalin 100 mg/1CapsuleOralViatris Specialty LLC58151-239
LyricapregabalinPregabalin 150 mg/1CapsuleOralViatris Specialty LLC58151-240
LyricapregabalinPregabalin 300 mg/1CapsuleOralViatris Specialty LLC58151-242
LyricapregabalinPregabalin 225 mg/1CapsuleOralViatris Specialty LLC58151-243

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