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United States · US · US:42385-979_5fd82a02-46ac-4312-a008-fa17e5cd3ffd

Gabapentin

Orange BookUNIISPLATC N02BF01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerLaurus Labs Limited
CountryUS (United States)
ATC codeN02BF01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    4238597901
    100 TABLET, FILM COATED in 1 BOTTLE (42385-979-01)
  • ndc11
    4238597905
    500 TABLET, FILM COATED in 1 BOTTLE (42385-979-05)
  • ndc11
    4238597911
    1000 TABLET, FILM COATED in 1 BOTTLE (42385-979-11)
  • ndc11
    4238597930
    30 TABLET, FILM COATED in 1 BOTTLE (42385-979-30)
  • ndc11
    4238597972
    10 BLISTER PACK in 1 CARTON (42385-979-72) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    4238597990
    90 TABLET, FILM COATED in 1 BOTTLE (42385-979-90)

Annotations

UNII (FDA Substance ID)
6CW7F3G59X
GABAPENTIN
RxCUI 25480
Orange Book
A217965
AB1AB1
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6CW7F3G59X",
    "rxcui": "25480",
    "inchikey": "UGJMXCAKCUNAIE-UHFFFAOYSA-N",
    "display_name": "GABAPENTIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "798575b9-ddfa-4915-9574-626abbaf025f": {
      "match": "brand_token",
      "title": "GABAPENTIN CAPSULE [STRIDES PHARMA SCIENCE LIMITED]",
      "spl_version": "3",
      "published_date": "2026-06-02"
    }
  },
  "productid": "42385-979_5fd82a02-46ac-4312-a008-fa17e5cd3ffd",
  "productndc": "42385-979",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "217965",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "600MG",
        "product_no": "001",
        "approval_date": "Apr 8, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Apr 8, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "GABAPENTIN",
  "proprietary_name": "Gabapentin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA217965",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Gabapentin",
  "start_marketing_date": "20240409",
  "active_numerator_strength": "600"
}

Related drugs

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