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 · 9

ndc11
7133504721
30 TABLET in 1 BOTTLE (71335-0472-1)
ndc11
7133504722
60 TABLET in 1 BOTTLE (71335-0472-2)
ndc11
7133504723
90 TABLET in 1 BOTTLE (71335-0472-3)
ndc11
7133504724
100 TABLET in 1 BOTTLE (71335-0472-4)
ndc11
7133504725
180 TABLET in 1 BOTTLE (71335-0472-5)
ndc11
7133504726
20 TABLET in 1 BOTTLE (71335-0472-6)
ndc11
7133504727
28 TABLET in 1 BOTTLE (71335-0472-7)
ndc11
7133504728
10 TABLET in 1 BOTTLE (71335-0472-8)
ndc11
7133504729
120 TABLET in 1 BOTTLE (71335-0472-9)

Annotations

UNII (FDA Substance ID)

F8A3652H1V

PROPRANOLOL HYDROCHLORIDE

RxCUI 82084

Orange Book

A070221

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": "71335-0472_5b7d1148-a500-43c2-aefd-b8ac3aa2e6bc",
  "productndc": "71335-0472",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "070221",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "80MG",
        "product_no": "001",
        "approval_date": "Apr 14, 1986"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Aug 1, 1986"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Aug 1, 1986"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "004",
        "approval_date": "Aug 1, 1986"
      },
      {
        "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": "ANDA070221",
  "marketing_category": "ANDA",
  "nonproprietary_name": "propranolol hydrochloride",
  "start_marketing_date": "20100621",
  "active_numerator_strength": "40"
}

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