Gabapentin NDC 63629-7306

Product information

Brand name (proprietary)

Gabapentin

Generic name (nonproprietary)

gabapentin

Active ingredients

Gabapentin — 300 mg/1

Dosage form

Capsule

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 078428

Marketing start

Nov 24, 2009

Listing expires

Dec 31, 2026

Other FDA classes

Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)

Identifiers

Product ID 63629-7306_f11fbdbf-9fbc-49ef-8296-44be1c9d7a03SPL ID f11fbdbf-9fbc-49ef-8296-44be1c9d7a03SPL set ID 506bf880-9564-404c-951a-703797ffdad8RxCUI 310431UNII 6CW7F3G59X

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

N463629730601 followed by a unit qualifier and the quantity Copy

Package 63629-7306-01. 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.

Other NDCs under ANDA 078428

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