Package 10702-150-16

Brand: hydrocodone bitartrate and homatropine methylbromide

Generic: hydrocodone bitartrate and homatropine methylbromide oral solution
NDC Package

Package Facts

Identity

Package NDC 10702-150-16
Digits Only 1070215016
Product NDC 10702-150
Description

473 mL in 1 BOTTLE (10702-150-16)

Marketing

Marketing Status
Marketed Since 2017-02-21
Brand hydrocodone bitartrate and homatropine methylbromide
Generic hydrocodone bitartrate and homatropine methylbromide oral solution
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47b998e5-ead4-9500-e063-6294a90a79ba", "openfda": {"unii": ["68JRS2HC1C", "NO70W886KK"], "rxcui": ["992668"], "spl_set_id": ["9a737416-08e0-4df6-897e-cf9d1b5f0b01"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (10702-150-16)", "package_ndc": "10702-150-16", "marketing_start_date": "20170221"}], "brand_name": "Hydrocodone Bitartrate and Homatropine Methylbromide", "product_id": "10702-150_47b998e5-ead4-9500-e063-6294a90a79ba", "dosage_form": "LIQUID", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "10702-150", "dea_schedule": "CII", "generic_name": "hydrocodone bitartrate and homatropine methylbromide oral solution", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Homatropine Methylbromide", "active_ingredients": [{"name": "HOMATROPINE METHYLBROMIDE", "strength": "1.5 mg/5mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/5mL"}], "application_number": "ANDA207487", "marketing_category": "ANDA", "marketing_start_date": "20170221", "listing_expiration_date": "20271231"}