Package 27808-049-01

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 27808-049-01
Digits Only 2780804901
Product NDC 27808-049
Product ID 27808-049_dc790b2b-c3f6-428c-83f0-0781ded05d6e
Description

473 mL in 1 BOTTLE, PLASTIC (27808-049-01)

Marketing

Marketing Status
Marketed Since 2022-12-30
Brand hydrocodone bitartrate and acetaminophen
Generic hydrocodone bitartrate and acetaminophen
Sample Package No

Linked Drug Pages (1)

Hydrocodone Bitartrate and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc790b2b-c3f6-428c-83f0-0781ded05d6e", "openfda": {"upc": ["0327808049018"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856940"], "spl_set_id": ["57e1fe79-eb60-4f4f-bb38-6df0270d408f"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (27808-049-01)", "package_ndc": "27808-049-01", "marketing_start_date": "20221230"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "27808-049_dc790b2b-c3f6-428c-83f0-0781ded05d6e", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "27808-049", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/15mL"}], "application_number": "ANDA201295", "marketing_category": "ANDA", "marketing_start_date": "20211230", "listing_expiration_date": "20271231"}