Propranolol Hydrochloride

In shortageOrange BookUNIISPLATC C07AA05

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeC07AA05

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133517121
20 TABLET in 1 BOTTLE (71335-1712-1)
ndc11
7133517122
30 TABLET in 1 BOTTLE (71335-1712-2)
ndc11
7133517123
100 TABLET in 1 BOTTLE (71335-1712-3)
ndc11
7133517124
60 TABLET in 1 BOTTLE (71335-1712-4)
ndc11
7133517125
90 TABLET in 1 BOTTLE (71335-1712-5)
ndc11
7133517126
180 TABLET in 1 BOTTLE (71335-1712-6)
ndc11
7133517127
28 TABLET in 1 BOTTLE (71335-1712-7)
ndc11
7133517128
10 TABLET in 1 BOTTLE (71335-1712-8)

Annotations

UNII (FDA Substance ID)

F8A3652H1V

PROPRANOLOL HYDROCHLORIDE

RxCUI 82084

Orange Book

A070322

ABABABABAB

DailyMed SPL labels

1 version tracked

FDA shortage

Currently in shortage

Propranolol Hydrochloride Injection

Raw payload (JSON)

{
  "unii": {
    "unii": "F8A3652H1V",
    "rxcui": "82084",
    "inchikey": "ZMRUPTIKESYGQW-UHFFFAOYSA-N",
    "display_name": "PROPRANOLOL HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4dd23053-0458-40f2-ac34-afb8cc9903aa": {
      "match": "brand_token",
      "title": "PROPRANOLOL HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "71335-1712_cf29d6a7-1e9e-478d-ac01-f178a7de9f7b",
  "productndc": "71335-1712",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "070322",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "80MG",
        "product_no": "001",
        "approval_date": "Aug 4, 1986"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Oct 22, 1985"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Oct 22, 1985"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "004",
        "approval_date": "Oct 22, 1985"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "60MG",
        "product_no": "005",
        "approval_date": "Sep 24, 1986"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PROPRANOLOL HYDROCHLORIDE",
  "shortage_reason": "Propranolol Hydrochloride Injection",
  "shortage_status": "current",
  "proprietary_name": "Propranolol Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA070322",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Propranolol Hydrochloride",
  "start_marketing_date": "20191031",
  "active_numerator_strength": "20"
}

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