cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler zydus pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1110
Product ID 70710-1110_b36a8686-4b30-4b42-a673-44cc58b775c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208938
Listing Expiration 2026-12-31
Marketing Start 2017-07-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101110
Hyphenated Format 70710-1110

Supplemental Identifiers

RxCUI
866144
UPC
0370710111014
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 ANDA208938 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (70710-1110-0)
  • 100 TABLET in 1 BOTTLE (70710-1110-1)
source: ndc

Packages (2)

70710-1110-0 1000 TABLET in 1 BOTTLE (70710-1110-0) 70710-1110-1 100 TABLET in 1 BOTTLE (70710-1110-1)

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": "b36a8686-4b30-4b42-a673-44cc58b775c3", "openfda": {"upc": ["0370710111014"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["766f9b59-2c72-45ac-af09-5dd6c3e16b52"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70710-1110-0)", "package_ndc": "70710-1110-0", "marketing_start_date": "20170720"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1110-1)", "package_ndc": "70710-1110-1", "marketing_start_date": "20170720"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70710-1110_b36a8686-4b30-4b42-a673-44cc58b775c3", "dosage_form": "TABLET", "product_ndc": "70710-1110", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA208938", "marketing_category": "ANDA", "marketing_start_date": "20170720", "listing_expiration_date": "20261231"}