Gabapentin

Orange BookUNIISPLATC N02BF01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN02BF01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 9

ndc11
7133527651
30 TABLET, FILM COATED in 1 BOTTLE (71335-2765-1)
ndc11
7133527652
60 TABLET, FILM COATED in 1 BOTTLE (71335-2765-2)
ndc11
7133527653
90 TABLET, FILM COATED in 1 BOTTLE (71335-2765-3)
ndc11
7133527654
180 TABLET, FILM COATED in 1 BOTTLE (71335-2765-4)
ndc11
7133527655
120 TABLET, FILM COATED in 1 BOTTLE (71335-2765-5)
ndc11
7133527656
100 TABLET, FILM COATED in 1 BOTTLE (71335-2765-6)
ndc11
7133527657
84 TABLET, FILM COATED in 1 BOTTLE (71335-2765-7)
ndc11
7133527658
112 TABLET, FILM COATED in 1 BOTTLE (71335-2765-8)
ndc11
7133527659
135 TABLET, FILM COATED in 1 BOTTLE (71335-2765-9)

Annotations

UNII (FDA Substance ID)

6CW7F3G59X

GABAPENTIN

RxCUI 25480

Orange Book

A200651

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": "71335-2765_5b6860be-3342-47b5-b38e-11c3e903b5cb",
  "productndc": "71335-2765",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "200651",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "600MG",
        "product_no": "001",
        "approval_date": "Oct 6, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Oct 6, 2011"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "GABAPENTIN",
  "proprietary_name": "Gabapentin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA200651",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Gabapentin",
  "start_marketing_date": "20111006",
  "active_numerator_strength": "800"
}

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