cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: strides pharma science limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler strides pharma science limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
Strides Pharma Science Limited

Identifiers & Regulatory

Product NDC 64380-795
Product ID 64380-795_54787424-10c7-40b3-b1ca-5a796572ad34
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209172
Listing Expiration 2026-12-31
Marketing Start 2018-04-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64380795
Hyphenated Format 64380-795

Supplemental Identifiers

RxCUI
866144
UPC
0364380795063
UNII
NJ82J0F8QC

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 cyproheptadine hydrochloride (source: ndc)
Generic Name cyproheptadine hydrochloride (source: ndc)
Application Number ANDA209172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (64380-795-06)
  • 1000 TABLET in 1 BOTTLE (64380-795-08)
source: ndc

Packages (2)

64380-795-06 100 TABLET in 1 BOTTLE (64380-795-06) 64380-795-08 1000 TABLET in 1 BOTTLE (64380-795-08)

Ingredients (1)

cyproheptadine hydrochloride (4 mg/1)

Linked Drug Pages (1)

CYPROHEPTADINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "54787424-10c7-40b3-b1ca-5a796572ad34", "openfda": {"upc": ["0364380795063"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["b28c2ca0-140d-44d8-a59e-75fbfe8eabdd"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64380-795-06)", "package_ndc": "64380-795-06", "marketing_start_date": "20180411"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64380-795-08)", "package_ndc": "64380-795-08", "marketing_start_date": "20180411"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "64380-795_54787424-10c7-40b3-b1ca-5a796572ad34", "dosage_form": "TABLET", "product_ndc": "64380-795", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA209172", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20261231"}