promethazine hydrochloride
Generic: promethazine hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
promethazine hydrochloride
Generic Name
promethazine hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Routes
Active Ingredients
promethazine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-5307
Product ID
0591-5307_4ad005c9-31b6-4232-995f-920d1839256e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA083426
Listing Expiration
2026-12-31
Marketing Start
1973-09-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915307
Hyphenated Format
0591-5307
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
ANDA083426 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (0591-5307-01)
- 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5307-10)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ad005c9-31b6-4232-995f-920d1839256e", "openfda": {"upc": ["0305915319019", "0305915307016"], "unii": ["R61ZEH7I1I"], "rxcui": ["992447", "992475"], "spl_set_id": ["a32255f0-0077-489e-bdc6-869aca8cd434"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-5307-01)", "package_ndc": "0591-5307-01", "marketing_start_date": "19730919"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0591-5307-10)", "package_ndc": "0591-5307-10", "marketing_start_date": "19730919"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0591-5307_4ad005c9-31b6-4232-995f-920d1839256e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0591-5307", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA083426", "marketing_category": "ANDA", "marketing_start_date": "19730919", "listing_expiration_date": "20261231"}