doxycycline hyclate

Generic: doxycycline hyclate

Labeler: alembic pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler alembic pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 20 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-352
Product ID 46708-352_994cfe3e-3b42-4837-b9fc-c88ba7484e51
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210537
Listing Expiration 2026-12-31
Marketing Start 2020-03-05

Pharmacologic Class

Classes
tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46708352
Hyphenated Format 46708-352

Supplemental Identifiers

RxCUI
283535
UPC
0346708352608
UNII
19XTS3T51U

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 doxycycline hyclate (source: ndc)
Generic Name doxycycline hyclate (source: ndc)
Application Number ANDA210537 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31)
  • 60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91)
source: ndc

Packages (3)

46708-352-31 100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31) 46708-352-60 60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60) 46708-352-91 1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91)

Ingredients (1)

doxycycline hyclate (20 mg/1)

Linked Drug Pages (1)

Doxycycline Hyclate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "994cfe3e-3b42-4837-b9fc-c88ba7484e51", "openfda": {"upc": ["0346708352608"], "unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["ec4535a1-69f0-40a2-bcba-11afc75c721d"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31)", "package_ndc": "46708-352-31", "marketing_start_date": "20200305"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60)", "package_ndc": "46708-352-60", "marketing_start_date": "20200305"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91)", "package_ndc": "46708-352-91", "marketing_start_date": "20200305"}], "brand_name": "Doxycycline Hyclate", "product_id": "46708-352_994cfe3e-3b42-4837-b9fc-c88ba7484e51", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "46708-352", "generic_name": "Doxycycline Hyclate", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "20 mg/1"}], "application_number": "ANDA210537", "marketing_category": "ANDA", "marketing_start_date": "20200305", "listing_expiration_date": "20261231"}