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 CAPSULE
Routes
ORAL
Active Ingredients

doxycycline 75 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 63304-615
Product ID 63304-615_338488d1-e9d8-6b00-e063-6294a90a37c0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065053
Listing Expiration 2026-12-31
Marketing Start 2000-12-26

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 63304615
Hyphenated Format 63304-615

Supplemental Identifiers

RxCUI
700408 1649401 1649990
UPC
0363304614015
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 ANDA065053 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (63304-615-01)
  • 500 CAPSULE in 1 BOTTLE (63304-615-05)
  • 1 BLISTER PACK in 1 CARTON (63304-615-11) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (3)

63304-615-01 100 CAPSULE in 1 BOTTLE (63304-615-01) 63304-615-05 500 CAPSULE in 1 BOTTLE (63304-615-05) 63304-615-11 1 BLISTER PACK in 1 CARTON (63304-615-11) / 1 CAPSULE in 1 BLISTER PACK

Ingredients (1)

doxycycline (75 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": "338488d1-e9d8-6b00-e063-6294a90a37c0", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0363304614015"], "unii": ["N12000U13O"], "rxcui": ["700408", "1649401", "1649990"], "spl_set_id": ["829dbd3d-5c2b-47b8-96a5-423af78c93b9"], "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": "100 CAPSULE in 1 BOTTLE (63304-615-01)", "package_ndc": "63304-615-01", "marketing_start_date": "20001226"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (63304-615-05)", "package_ndc": "63304-615-05", "marketing_start_date": "20001226"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63304-615-11)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "63304-615-11", "marketing_start_date": "20001226"}], "brand_name": "Doxycycline", "product_id": "63304-615_338488d1-e9d8-6b00-e063-6294a90a37c0", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63304-615", "generic_name": "Doxycycline", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "75 mg/1"}], "application_number": "ANDA065053", "marketing_category": "ANDA", "marketing_start_date": "20001226", "listing_expiration_date": "20261231"}