promethazine hydrochloride
Generic: promethazine hydrochloride
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
promethazine hydrochloride
Generic Name
promethazine hydrochloride
Labeler
camber pharmaceuticals, inc.
Dosage Form
SUPPOSITORY
Routes
Active Ingredients
promethazine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
31722-041
Product ID
31722-041_ecb3a4da-a4fc-7803-e053-2a95a90a0f3f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216446
Listing Expiration
2026-12-31
Marketing Start
2022-11-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722041
Hyphenated Format
31722-041
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
promethazine hydrochloride (source: ndc)
Generic Name
promethazine hydrochloride (source: ndc)
Application Number
ANDA216446 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (31722-041-31) / 6 SUPPOSITORY in 1 BLISTER PACK
Packages (1)
Ingredients (1)
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 (31722-041-31) / 6 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "31722-041-31", "marketing_start_date": "20221102"}], "brand_name": "Promethazine Hydrochloride", "product_id": "31722-041_ecb3a4da-a4fc-7803-e053-2a95a90a0f3f", "dosage_form": "SUPPOSITORY", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "31722-041", "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": "25 mg/1"}], "application_number": "ANDA216446", "marketing_category": "ANDA", "marketing_start_date": "20221102", "listing_expiration_date": "20261231"}