propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-609
Product ID 60687-609_2205da94-02fb-4a72-e063-6294a90a396e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070322
Listing Expiration 2026-12-31
Marketing Start 2021-12-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687609
Hyphenated Format 60687-609

Supplemental Identifiers

RxCUI
856448 856457 856519
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
  • 40 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-609-01) / 1 TABLET in 1 BLISTER PACK (60687-609-11)
source: ndc

Packages (1)

60687-609-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-609-01) / 1 TABLET in 1 BLISTER PACK (60687-609-11)

Ingredients (1)

propranolol hydrochloride (40 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": "2205da94-02fb-4a72-e063-6294a90a396e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519"], "spl_set_id": ["d027f39e-7648-44c8-a8dc-b26b4cdd81be"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-609-01)  / 1 TABLET in 1 BLISTER PACK (60687-609-11)", "package_ndc": "60687-609-01", "marketing_start_date": "20211209"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60687-609_2205da94-02fb-4a72-e063-6294a90a396e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-609", "generic_name": "Propranolol Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20211209", "listing_expiration_date": "20261231"}