Package 31722-040-31
Brand: promethazine hydrochloride
Generic: promethazine hydrochloridePackage Facts
Identity
Package NDC
31722-040-31
Digits Only
3172204031
Product NDC
31722-040
Description
2 BLISTER PACK in 1 CARTON (31722-040-31) / 6 SUPPOSITORY in 1 BLISTER PACK
Marketing
Marketing Status
Brand
promethazine hydrochloride
Generic
promethazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "ecb3a4da-a4fc-7803-e053-2a95a90a0f3f", "openfda": {"upc": ["0331722040310", "0331722041317"], "unii": ["R61ZEH7I1I"], "rxcui": ["992441", "992454"], "spl_set_id": ["ba7d9e82-9b13-4607-b2f9-25e575b8c73b"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (31722-040-31) / 6 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "31722-040-31", "marketing_start_date": "20221102"}], "brand_name": "Promethazine Hydrochloride", "product_id": "31722-040_ecb3a4da-a4fc-7803-e053-2a95a90a0f3f", "dosage_form": "SUPPOSITORY", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "31722-040", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA216446", "marketing_category": "ANDA", "marketing_start_date": "20221102", "listing_expiration_date": "20261231"}