Medroxyprogesterone Acetate

Orange BookUNIISPLATC L02AB02

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

Identification

ManufacturerProficient Rx LP

CountryUS (United States)

ATC codeL02AB02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
6318738210
10 TABLET in 1 BOTTLE (63187-382-10)
ndc11
6318738220
20 TABLET in 1 BOTTLE (63187-382-20)
ndc11
6318738230
30 TABLET in 1 BOTTLE (63187-382-30)
ndc11
6318738240
40 TABLET in 1 BOTTLE (63187-382-40)
ndc11
6318738260
60 TABLET in 1 BOTTLE (63187-382-60)
ndc11
6318738290
90 TABLET in 1 BOTTLE (63187-382-90)

Annotations

UNII (FDA Substance ID)

C2QI4IOI2G

MEDROXYPROGESTERONE ACETATE

RxCUI 1000112

Orange Book

A040159

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "C2QI4IOI2G",
    "rxcui": "1000112",
    "inchikey": "PSGAAPLEWMOORI-PEINSRQWSA-N",
    "display_name": "MEDROXYPROGESTERONE ACETATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1020bb60-4f13-4cd7-aaa1-c556752c84b7": {
      "match": "brand_token",
      "title": "MEDROXYPROGESTERONE ACETATE TABLET [REMEDYREPACK INC.]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "63187-382_867e0dca-0472-415c-97f5-340123e86116",
  "productndc": "63187-382",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040159",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "001",
        "approval_date": "Aug 9, 1996"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "002",
        "approval_date": "Aug 9, 1996"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "003",
        "approval_date": "Aug 9, 1996"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MEDROXYPROGESTERONE ACETATE",
  "proprietary_name": "Medroxyprogesterone Acetate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040159",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Medroxyprogesterone Acetate",
  "start_marketing_date": "19961204",
  "active_numerator_strength": "10"
}

Related drugs

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