doxycycline hyclate

Generic: doxycycline hyclate

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

Drug Facts

Product Profile

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

doxycycline hyclate 150 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-388
Product ID 62332-388_23a5f41d-9033-4744-9ac4-e2e3fe39e6b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211744
Listing Expiration 2026-12-31
Marketing Start 2020-06-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332388
Hyphenated Format 62332-388

Supplemental Identifiers

RxCUI
1649425 1650446
UPC
0362332388608 0362332387601
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 ANDA211744 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (62332-388-60)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-388-91)
source: ndc

Packages (2)

62332-388-60 60 TABLET, FILM COATED in 1 BOTTLE (62332-388-60) 62332-388-91 1000 TABLET, FILM COATED in 1 BOTTLE (62332-388-91)

Ingredients (1)

doxycycline hyclate (150 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": "23a5f41d-9033-4744-9ac4-e2e3fe39e6b5", "openfda": {"upc": ["0362332388608", "0362332387601"], "unii": ["19XTS3T51U"], "rxcui": ["1649425", "1650446"], "spl_set_id": ["cec4368f-2852-443d-9d6f-7ba95807021b"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62332-388-60)", "package_ndc": "62332-388-60", "marketing_start_date": "20200630"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-388-91)", "package_ndc": "62332-388-91", "marketing_start_date": "20200630"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "62332-388_23a5f41d-9033-4744-9ac4-e2e3fe39e6b5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62332-388", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "150 mg/1"}], "application_number": "ANDA211744", "marketing_category": "ANDA", "marketing_start_date": "20200630", "listing_expiration_date": "20261231"}