doxycycline

Generic: doxycycline

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

Drug Facts

Product Profile

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

doxycycline 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0213
Product ID 70518-0213_47e5076b-5309-a2f6-e063-6394a90ae830
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204234
Listing Expiration 2027-12-31
Marketing Start 2017-02-10

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 705180213
Hyphenated Format 70518-0213

Supplemental Identifiers

RxCUI
1649990
UNII
N12000U13O
NUI
N0000175882 N0000007948

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 ANDA204234 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-0213-0)
  • 20 CAPSULE in 1 BLISTER PACK (70518-0213-1)
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-0213-2)
  • 20 CAPSULE in 1 BOTTLE, PLASTIC (70518-0213-3)
  • 14 CAPSULE in 1 BLISTER PACK (70518-0213-7)
source: ndc

Packages (5)

Ingredients (1)

doxycycline (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e5076b-5309-a2f6-e063-6394a90ae830", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1649990"], "spl_set_id": ["fa2d9328-b688-47af-8c4d-dc328cf35392"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0213-0)", "package_ndc": "70518-0213-0", "marketing_start_date": "20170210"}, {"sample": false, "description": "20 CAPSULE in 1 BLISTER PACK (70518-0213-1)", "package_ndc": "70518-0213-1", "marketing_start_date": "20170210"}, {"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (70518-0213-2)", "package_ndc": "70518-0213-2", "marketing_start_date": "20170531"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE, PLASTIC (70518-0213-3)", "package_ndc": "70518-0213-3", "marketing_start_date": "20170717"}, {"sample": false, "description": "14 CAPSULE in 1 BLISTER PACK (70518-0213-7)", "package_ndc": "70518-0213-7", "marketing_start_date": "20200317"}], "brand_name": "DOXYCYCLINE", "product_id": "70518-0213_47e5076b-5309-a2f6-e063-6394a90ae830", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-0213", "generic_name": "DOXYCYCLINE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA204234", "marketing_category": "ANDA", "marketing_start_date": "20170210", "listing_expiration_date": "20271231"}