doxycycline

Generic: doxycycline

Labeler: sun pharmaceutical industries inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler sun pharmaceutical industries inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline 50 mg/1

Manufacturer
Sun Pharmaceutical Industries Inc.

Identifiers & Regulatory

Product NDC 63304-130
Product ID 63304-130_fd417a50-69b5-40b4-89fd-58aea77ab547
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065356
Listing Expiration 2026-12-31
Marketing Start 2018-08-06

Pharmacologic Class

Established (EPC)
tetracycline-class drug [epc]
Chemical Structure
tetracyclines [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63304130
Hyphenated Format 63304-130

Supplemental Identifiers

RxCUI
1649429 1650142 1650444 1652673
UPC
0363304173307
UNII
N12000U13O
NUI
N0000175882 N0000007948

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 ANDA065356 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)
source: ndc

Packages (1)

63304-130-10 1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)

Ingredients (1)

doxycycline (50 mg/1)

Linked Drug Pages (1)

Doxycycline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fd417a50-69b5-40b4-89fd-58aea77ab547", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0363304173307"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["8224b9c5-5c4b-4dda-bc58-47b6604c2884"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)", "package_ndc": "63304-130-10", "marketing_start_date": "20180806"}], "brand_name": "Doxycycline", "product_id": "63304-130_fd417a50-69b5-40b4-89fd-58aea77ab547", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63304-130", "generic_name": "Doxycycline", "labeler_name": "Sun Pharmaceutical Industries Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "50 mg/1"}], "application_number": "ANDA065356", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}