azithromycin

Generic: azithromycin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azithromycin
Generic Name azithromycin
Labeler proficient rx lp
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

azithromycin dihydrate 200 mg/5mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-216
Product ID 71205-216_476af655-9fb8-4253-a569-fb3295680838
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211147
Listing Expiration 2026-12-31
Marketing Start 2018-08-06

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205216
Hyphenated Format 71205-216

Supplemental Identifiers

RxCUI
141963
UPC
0371205216306
UNII
5FD1131I7S

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 azithromycin (source: ndc)
Generic Name azithromycin (source: ndc)
Application Number ANDA211147 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (71205-216-30) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

azithromycin dihydrate (200 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "476af655-9fb8-4253-a569-fb3295680838", "openfda": {"upc": ["0371205216306"], "unii": ["5FD1131I7S"], "rxcui": ["141963"], "spl_set_id": ["33140df5-420d-469f-b6c8-121e952a5cb6"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71205-216-30)  / 30 mL in 1 BOTTLE", "package_ndc": "71205-216-30", "marketing_start_date": "20190201"}], "brand_name": "Azithromycin", "product_id": "71205-216_476af655-9fb8-4253-a569-fb3295680838", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-216", "generic_name": "Azithromycin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "200 mg/5mL"}], "application_number": "ANDA211147", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}