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United States Β· US Β· US:71335-1840_629f541a-8b78-48b2-bb97-1b072195dd83

PHENDIMETRAZINE TARTRATE

Orange BookUNIISPL

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 10

  • ndc11
    7133518400
    120 TABLET in 1 BOTTLE (71335-1840-0)
  • ndc11
    7133518401
    30 TABLET in 1 BOTTLE (71335-1840-1)
  • ndc11
    7133518402
    90 TABLET in 1 BOTTLE (71335-1840-2)
  • ndc11
    7133518403
    15 TABLET in 1 BOTTLE (71335-1840-3)
  • ndc11
    7133518404
    60 TABLET in 1 BOTTLE (71335-1840-4)
  • ndc11
    7133518405
    7 TABLET in 1 BOTTLE (71335-1840-5)
  • ndc11
    7133518406
    21 TABLET in 1 BOTTLE (71335-1840-6)
  • ndc11
    7133518407
    42 TABLET in 1 BOTTLE (71335-1840-7)
  • ndc11
    7133518408
    100 TABLET in 1 BOTTLE (71335-1840-8)
  • ndc11
    7133518409
    28 TABLET in 1 BOTTLE (71335-1840-9)

Annotations

UNII (FDA Substance ID)
6985IP0T80
PHENDIMETRAZINE TARTRATE
RxCUI 58157
Orange Book
A085588
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6985IP0T80",
    "rxcui": "58157",
    "inchikey": "VEPOHXYIFQMVHW-PVJVQHJQSA-N",
    "display_name": "PHENDIMETRAZINE TARTRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f5c30a88-5814-5b42-e053-2995a90a437a": {
      "match": "brand_token",
      "title": "PHENDIMETRAZINE TARTRATE TABLET [CALVIN SCOTT & CO., INC.]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-1840_629f541a-8b78-48b2-bb97-1b072195dd83",
  "productndc": "71335-1840",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "085588",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "35MG",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PHENDIMETRAZINE TARTRATE",
  "proprietary_name": "PHENDIMETRAZINE TARTRATE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA085588",
  "marketing_category": "ANDA",
  "nonproprietary_name": "PHENDIMETRAZINE TARTRATE",
  "start_marketing_date": "20180701",
  "active_numerator_strength": "35"
}

Access this data programmatically

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PHENDIMETRAZINE TARTRATE (US) β€” Drug Database