propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: pharmaceutical associates, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler pharmaceutical associates, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/5mL

Manufacturer
Pharmaceutical Associates, Inc.

Identifiers & Regulatory

Product NDC 0121-0908
Product ID 0121-0908_e20b8c76-152c-9fee-e053-2a95a90aa52d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070979
Listing Expiration 2026-12-31
Marketing Start 2021-09-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01210908
Hyphenated Format 0121-0908

Supplemental Identifiers

RxCUI
856724
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 ANDA070979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/5mL
source: ndc
Packaging
  • 4 TRAY in 1 CASE (0121-0908-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0908-05)
source: ndc

Packages (1)

0121-0908-40 4 TRAY in 1 CASE (0121-0908-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0908-05)

Ingredients (1)

propranolol hydrochloride (20 mg/5mL)

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e20b8c76-152c-9fee-e053-2a95a90aa52d", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856724"], "spl_set_id": ["ec5c919b-05d1-45d2-a6e4-ac4ae1101dbb"], "manufacturer_name": ["Pharmaceutical Associates, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TRAY in 1 CASE (0121-0908-40)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0908-05)", "package_ndc": "0121-0908-40", "marketing_start_date": "20210903"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0121-0908_e20b8c76-152c-9fee-e053-2a95a90aa52d", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0121-0908", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Pharmaceutical Associates, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA070979", "marketing_category": "ANDA", "marketing_start_date": "20210903", "listing_expiration_date": "20261231"}