NDC codes

FDA NDC Directory
Product NDC (as listed)58151-247Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58151-0247Add 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
58151-247-935815102479330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58151-247-93)Marketed from Jul 11, 2024

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)
Lyrica CR
Generic name (nonproprietary)
pregabalin
Active ingredients
Pregabalin — 330 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Viatris Specialty LLCNDC labeler code 58151
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 209501
Marketing start
Listing expires
DEA schedule
CV
Identifiers
Product ID 58151-247_67715d17-5ade-44ba-a5db-ba20d30d6da1SPL ID 67715d17-5ade-44ba-a5db-ba20d30d6da1SPL set ID f280bbd8-2af2-444a-bd96-e409337ca6ddRxCUI 1988974, 1988977, 1988980, 1994389, 1994392, 1994395UNII 55JG375S6M

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

N458151024793 followed by a unit qualifier and the quantity

Package 58151-0247-93. 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 CR is indicated for the management of: • Neuropathic pain associated with diabetic peripheral neuropathy • Postherpetic neuralgia Efficacy of LYRICA CR has not been established for the management of fibromyalgia or as adjunctive therapy for adult patients with partial onset seizures. LYRICA CR is indicated for the management of: • Neuropathic pain associated with diabetic peripheral neuropathy (DPN) ( 1 ) • Postherpetic neuralgia (PHN) ( 1 ) Efficacy of LYRICA CR has not been established for the management of fibromyalgia or as adjunctive therapy for adult patients with partial onset seizures.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58151-247

What is NDC 58151-247?
58151-247 is the product NDC for Lyrica CR (pregabalin), Pregabalin 330 mg/1 tablet, film coated, extended release, listed with the FDA by Viatris Specialty LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lyrica CR (Pregabalin).
What is the active ingredient?
Pregabalin.
Who is the labeler?
Viatris Specialty LLC, NDC labeler code 58151. 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 CR?
2 other product NDCs are listed under this name. See all Lyrica CR 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 CR NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lyrica CRpregabalinPregabalin 165 mg/1Tablet, Film coated, Extended releaseOralViatris Specialty LLC58151-24658151-0246-93
Lyrica CRpregabalinPregabalin 82.5 mg/1Tablet, Film coated, Extended releaseOralViatris Specialty LLC58151-24558151-0245-93

Other NDCs under NDA 209501

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

FDA NDC Directory listings under NDA 209501
ProductStrengthForm · routeLabelerProduct NDC
Lyrica CRpregabalinPregabalin 165 mg/1Tablet, Film coated, Extended releaseOralViatris Specialty LLC58151-246
Lyrica CRpregabalinPregabalin 82.5 mg/1Tablet, Film coated, Extended releaseOralViatris Specialty LLC58151-245

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Lyrica CR NDC 58151-247 | National Drug Code | Med-Code