doxycycline hyclate

Generic: doxycycline hyclate

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

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1248
Product ID 70518-1248_48c308d7-e6d7-7c36-e063-6394a90ac911
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062676
Listing Expiration 2027-12-31
Marketing Start 2018-06-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181248
Hyphenated Format 70518-1248

Supplemental Identifiers

RxCUI
1649988
UNII
19XTS3T51U

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 ANDA062676 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-1248-0)
source: ndc

Packages (1)

Ingredients (1)

doxycycline hyclate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c308d7-e6d7-7c36-e063-6394a90ac911", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1649988"], "spl_set_id": ["6e3d0691-c071-441c-9b00-22a380305066"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (70518-1248-0)", "package_ndc": "70518-1248-0", "marketing_start_date": "20180608"}], "brand_name": "Doxycycline Hyclate", "product_id": "70518-1248_48c308d7-e6d7-7c36-e063-6394a90ac911", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-1248", "generic_name": "Doxycycline Hyclate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062676", "marketing_category": "ANDA", "marketing_start_date": "20180608", "listing_expiration_date": "20271231"}