tetracycline hydrochloride
Generic: tetracycline hydrochloride
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
tetracycline hydrochloride
Generic Name
tetracycline hydrochloride
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
tetracycline hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
23155-767
Product ID
23155-767_8e073e02-ee9f-402e-894f-97b2c0b4dfef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062752
Listing Expiration
2026-12-31
Marketing Start
2020-04-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155767
Hyphenated Format
23155-767
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
tetracycline hydrochloride (source: ndc)
Generic Name
tetracycline hydrochloride (source: ndc)
Application Number
ANDA062752 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (23155-767-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e073e02-ee9f-402e-894f-97b2c0b4dfef", "openfda": {"unii": ["P6R62377KV"], "rxcui": ["198250", "198252"], "spl_set_id": ["3ce3e8dc-7fbd-4f8d-a65f-092e1ef21725"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (23155-767-01)", "package_ndc": "23155-767-01", "marketing_start_date": "20200401"}], "brand_name": "Tetracycline Hydrochloride", "product_id": "23155-767_8e073e02-ee9f-402e-894f-97b2c0b4dfef", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "23155-767", "generic_name": "Tetracycline Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tetracycline Hydrochloride", "active_ingredients": [{"name": "TETRACYCLINE HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA062752", "marketing_category": "ANDA", "marketing_start_date": "20200401", "listing_expiration_date": "20261231"}