propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 10 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3102
Product ID 70518-3102_4bceaf8b-7301-9096-e063-6294a90a81cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070322
Listing Expiration 2027-12-31
Marketing Start 2021-05-26

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183102
Hyphenated Format 70518-3102

Supplemental Identifiers

RxCUI
856448
UNII
F8A3652H1V

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name propranolol hydrochloride (source: ndc)
Generic Name propranolol hydrochloride (source: ndc)
Application Number ANDA070322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3102-0)
  • 30 TABLET in 1 BLISTER PACK (70518-3102-1)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-3)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-4)
source: ndc

Packages (4)

70518-3102-0 30 TABLET in 1 BLISTER PACK (70518-3102-0) 70518-3102-1 30 TABLET in 1 BLISTER PACK (70518-3102-1) 70518-3102-3 90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-3) 70518-3102-4 90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-4)

Ingredients (1)

propranolol hydrochloride (10 mg/1)

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bceaf8b-7301-9096-e063-6294a90a81cf", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["07c3fcab-33fe-4a6a-ba67-2d042190c146"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3102-0)", "package_ndc": "70518-3102-0", "marketing_start_date": "20210526"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3102-1)", "package_ndc": "70518-3102-1", "marketing_start_date": "20220825"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-3)", "package_ndc": "70518-3102-3", "marketing_start_date": "20240417"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-4)", "package_ndc": "70518-3102-4", "marketing_start_date": "20250416"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-3102_4bceaf8b-7301-9096-e063-6294a90a81cf", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3102", "generic_name": "Propranolol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20271231"}