doxycycline

Generic: doxycycline

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

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler zydus pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

doxycycline hyclate 200 mg/20mL

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 68382-911
Product ID 68382-911_b99072cd-f6d8-4d24-9014-f76e327dd6d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207757
Listing Expiration 2026-12-31
Marketing Start 2018-02-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68382911
Hyphenated Format 68382-911

Supplemental Identifiers

RxCUI
310027 1998483
UPC
0368382911018
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 (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA207757 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 mg/20mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (68382-911-01) / 20 mL in 1 VIAL
source: ndc

Packages (1)

68382-911-01 1 VIAL in 1 CARTON (68382-911-01) / 20 mL in 1 VIAL

Ingredients (1)

doxycycline hyclate (200 mg/20mL)

Linked Drug Pages (1)

Doxycycline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "b99072cd-f6d8-4d24-9014-f76e327dd6d3", "openfda": {"upc": ["0368382911018"], "unii": ["19XTS3T51U"], "rxcui": ["310027", "1998483"], "spl_set_id": ["7ce80f6e-3c0d-4978-b626-5fd3f3ff349e"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68382-911-01)  / 20 mL in 1 VIAL", "package_ndc": "68382-911-01", "marketing_start_date": "20180201"}], "brand_name": "Doxycycline", "product_id": "68382-911_b99072cd-f6d8-4d24-9014-f76e327dd6d3", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68382-911", "generic_name": "Doxycycline", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "200 mg/20mL"}], "application_number": "ANDA207757", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}