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United States · US · US:71205-931_26bd4975-008b-4029-b0da-3a75b0f7e0f4

Gabapentin

Orange BookUNIISPLATC N02BF01

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

Identification

ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeN02BF01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7120593100
    100 TABLET in 1 BOTTLE (71205-931-00)
  • ndc11
    7120593130
    30 TABLET in 1 BOTTLE (71205-931-30)
  • ndc11
    7120593155
    500 TABLET in 1 BOTTLE (71205-931-55)
  • ndc11
    7120593160
    60 TABLET in 1 BOTTLE (71205-931-60)
  • ndc11
    7120593164
    240 TABLET in 1 BOTTLE (71205-931-64)
  • ndc11
    7120593167
    270 TABLET in 1 BOTTLE (71205-931-67)
  • ndc11
    7120593172
    120 TABLET in 1 BOTTLE (71205-931-72)
  • ndc11
    7120593176
    360 TABLET in 1 BOTTLE (71205-931-76)
  • ndc11
    7120593178
    180 TABLET in 1 BOTTLE (71205-931-78)
  • ndc11
    7120593190
    90 TABLET in 1 BOTTLE (71205-931-90)

Annotations

UNII (FDA Substance ID)
6CW7F3G59X
GABAPENTIN
RxCUI 25480
Orange Book
A205101
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": "71205-931_26bd4975-008b-4029-b0da-3a75b0f7e0f4",
  "productndc": "71205-931",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "205101",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "600MG",
        "product_no": "001",
        "approval_date": "Feb 4, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Feb 4, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "GABAPENTIN",
  "proprietary_name": "Gabapentin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205101",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Gabapentin",
  "start_marketing_date": "20160411",
  "active_numerator_strength": "600"
}

Related drugs

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