Package 68071-4737-6

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4737-6
Digits Only 6807147376
Product NDC 68071-4737
Product ID 68071-4737_1aba0532-8f0c-d8df-e063-6294a90a6f45
Description

6 TABLET in 1 BOTTLE (68071-4737-6)

Marketing

Marketing Status
Marketed Since 2019-01-25
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

PROMETHAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1aba0532-8f0c-d8df-e063-6294a90a6f45", "openfda": {"upc": ["0368071473766"], "unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["804e2525-d61f-7bed-e053-2991aa0a5daa"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-4737-6)", "package_ndc": "68071-4737-6", "marketing_start_date": "20190125"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "68071-4737_1aba0532-8f0c-d8df-e063-6294a90a6f45", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68071-4737", "generic_name": "promethazine hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20060731", "listing_expiration_date": "20261231"}