doxylamine succinate and pyridoxine hydrochloride

Generic: doxylamine succinate and pyridoxine hydrochloride

Labeler: analog pharma
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name doxylamine succinate and pyridoxine hydrochloride
Generic Name doxylamine succinate and pyridoxine hydrochloride
Labeler analog pharma
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

doxylamine succinate 10 mg/1, pyridoxine hydrochloride 10 mg/1

Manufacturer
Analog Pharma

Identifiers & Regulatory

Product NDC 70505-100
Product ID 70505-100_59e091eb-f626-4083-b134-8d648d28b918
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021876
Listing Expiration 2026-12-31
Marketing Start 2018-11-15

Pharmacologic Class

Classes
analogs/derivatives [chemical/ingredient] antihistamine [epc] histamine receptor antagonists [moa] vitamin b 6 [chemical/ingredient] vitamin b6 analog [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70505100
Hyphenated Format 70505-100

Supplemental Identifiers

RxCUI
1375948
UNII
V9BI9B5YI2 68Y4CF58BV

Packaging Origin

Original Packager
true

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 doxylamine succinate and pyridoxine hydrochloride (source: ndc)
Generic Name doxylamine succinate and pyridoxine hydrochloride (source: ndc)
Application Number NDA021876 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (70505-100-10)
source: ndc

Packages (1)

70505-100-10 100 TABLET, DELAYED RELEASE in 1 BOTTLE (70505-100-10)

Ingredients (2)

doxylamine succinate (10 mg/1) pyridoxine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Doxylamine succinate and pyridoxine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "59e091eb-f626-4083-b134-8d648d28b918", "openfda": {"unii": ["V9BI9B5YI2", "68Y4CF58BV"], "rxcui": ["1375948"], "spl_set_id": ["76d10d65-0279-4e86-8104-cade4343f839"], "manufacturer_name": ["Analog Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (70505-100-10)", "package_ndc": "70505-100-10", "marketing_start_date": "20181115"}], "brand_name": "Doxylamine succinate and pyridoxine hydrochloride", "product_id": "70505-100_59e091eb-f626-4083-b134-8d648d28b918", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Analogs/Derivatives [Chemical/Ingredient]", "Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Vitamin B 6 [Chemical/Ingredient]", "Vitamin B6 Analog [EPC]"], "product_ndc": "70505-100", "generic_name": "Doxylamine succinate and pyridoxine hydrochloride", "labeler_name": "Analog Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxylamine succinate and pyridoxine hydrochloride", "active_ingredients": [{"name": "DOXYLAMINE SUCCINATE", "strength": "10 mg/1"}, {"name": "PYRIDOXINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA021876", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20181115", "listing_expiration_date": "20261231"}