promethazine hydrochloride and dextromethorphan hydrobromide oral solution
Generic: promethazine hydrochloride and dextromethorphan hydrobromide oral solution
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
promethazine hydrochloride and dextromethorphan hydrobromide oral solution
Generic Name
promethazine hydrochloride and dextromethorphan hydrobromide oral solution
Labeler
proficient rx lp
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 15 mg/5mL, promethazine hydrochloride 6.25 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71205-654
Product ID
71205-654_68a4c521-6db0-4e94-9906-96e96e251301
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040649
Listing Expiration
2026-12-31
Marketing Start
2020-10-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205654
Hyphenated Format
71205-654
Supplemental Identifiers
RxCUI
UPC
UNII
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 and dextromethorphan hydrobromide oral solution (source: ndc)
Generic Name
promethazine hydrochloride and dextromethorphan hydrobromide oral solution (source: ndc)
Application Number
ANDA040649 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/5mL
- 6.25 mg/5mL
Packaging
- 118 mL in 1 BOTTLE (71205-654-04)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "68a4c521-6db0-4e94-9906-96e96e251301", "openfda": {"upc": ["0371205654047"], "unii": ["9D2RTI9KYH", "R61ZEH7I1I"], "rxcui": ["991528"], "spl_set_id": ["68a4c521-6db0-4e94-9906-96e96e251301"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (71205-654-04)", "package_ndc": "71205-654-04", "marketing_start_date": "20220426"}], "brand_name": "Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution", "product_id": "71205-654_68a4c521-6db0-4e94-9906-96e96e251301", "dosage_form": "SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "71205-654", "generic_name": "Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/5mL"}, {"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "6.25 mg/5mL"}], "application_number": "ANDA040649", "marketing_category": "ANDA", "marketing_start_date": "20201005", "listing_expiration_date": "20261231"}