propranolol hydrochloride
Generic: propranolol hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
propranolol hydrochloride
Generic Name
propranolol hydrochloride
Labeler
american health packaging
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
propranolol hydrochloride 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-226
Product ID
60687-226_3f2c1ac2-1bb2-3613-e063-6394a90a211f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078703
Listing Expiration
2026-12-31
Marketing Start
2017-07-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687226
Hyphenated Format
60687-226
Supplemental Identifiers
RxCUI
UNII
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
ANDA078703 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-226-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-226-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f2c1ac2-1bb2-3613-e063-6394a90a211f", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856535", "856569"], "spl_set_id": ["015b5e4f-3228-4259-b419-e0e49694a058"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-226-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-226-11)", "package_ndc": "60687-226-01", "marketing_start_date": "20170714"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60687-226_3f2c1ac2-1bb2-3613-e063-6394a90a211f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-226", "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": "80 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20170714", "listing_expiration_date": "20261231"}