Package 60760-992-30

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-992-30
Digits Only 6076099230
Product NDC 60760-992
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-992-30)

Marketing

Marketing Status
Marketed Since 2025-04-15
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32d71d7e-3c77-6b63-e063-6294a90adaed", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["32d72d7b-5881-f431-e063-6394a90a3547"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-992-30)", "package_ndc": "60760-992-30", "marketing_start_date": "20250415"}], "brand_name": "clonidine hydrochloride", "product_id": "60760-992_32d71d7e-3c77-6b63-e063-6294a90adaed", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "60760-992", "generic_name": "clonidine hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20201224", "listing_expiration_date": "20261231"}