Package 0121-0908-40
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
0121-0908-40
Digits Only
0121090840
Product NDC
0121-0908
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)
Marketing
Marketing Status
Brand
propranolol hydrochloride
Generic
propranolol hydrochloride
Sample Package
No
Linked Drug Pages (1)
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"}