doxycycline

Generic: doxycycline

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler zydus lifesciences limited
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

doxycycline hyclate 200 mg/20mL

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1122
Product ID 70771-1122_6782ec89-eb1e-4283-9b02-b9fda4793cd3
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 707711122
Hyphenated Format 70771-1122

Supplemental Identifiers

RxCUI
310027 1998483
UPC
0370771112111 0370771112210
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 (70771-1122-1) / 20 mL in 1 VIAL
source: ndc

Packages (1)

70771-1122-1 1 VIAL in 1 CARTON (70771-1122-1) / 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": "6782ec89-eb1e-4283-9b02-b9fda4793cd3", "openfda": {"upc": ["0370771112111", "0370771112210"], "unii": ["19XTS3T51U"], "rxcui": ["310027", "1998483"], "spl_set_id": ["6ae11b4e-1c13-440b-a050-d76e062b0f92"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70771-1122-1)  / 20 mL in 1 VIAL", "package_ndc": "70771-1122-1", "marketing_start_date": "20180201"}], "brand_name": "Doxycycline", "product_id": "70771-1122_6782ec89-eb1e-4283-9b02-b9fda4793cd3", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70771-1122", "generic_name": "Doxycycline", "labeler_name": "Zydus Lifesciences Limited", "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"}