terbutaline sulfate

Generic: terbutaline sulfate

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

Drug Facts

Product Profile

Brand Name terbutaline sulfate
Generic Name terbutaline sulfate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

terbutaline sulfate 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-939
Product ID 71205-939_9f8ee6b8-61e1-478a-90de-57358fdb5905
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211832
Listing Expiration 2026-12-31
Marketing Start 2020-07-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205939
Hyphenated Format 71205-939

Supplemental Identifiers

RxCUI
857677 857683
UPC
0371205939304 0371205938307
UNII
576PU70Y8E

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 terbutaline sulfate (source: ndc)
Generic Name terbutaline sulfate (source: ndc)
Application Number ANDA211832 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71205-939-00)
  • 30 TABLET in 1 BOTTLE (71205-939-30)
  • 500 TABLET in 1 BOTTLE (71205-939-55)
  • 60 TABLET in 1 BOTTLE (71205-939-60)
  • 90 TABLET in 1 BOTTLE (71205-939-90)
source: ndc

Packages (5)

71205-939-00 100 TABLET in 1 BOTTLE (71205-939-00) 71205-939-30 30 TABLET in 1 BOTTLE (71205-939-30) 71205-939-55 500 TABLET in 1 BOTTLE (71205-939-55) 71205-939-60 60 TABLET in 1 BOTTLE (71205-939-60) 71205-939-90 90 TABLET in 1 BOTTLE (71205-939-90)

Ingredients (1)

terbutaline sulfate (5 mg/1)

Linked Drug Pages (1)

Terbutaline Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9f8ee6b8-61e1-478a-90de-57358fdb5905", "openfda": {"upc": ["0371205939304", "0371205938307"], "unii": ["576PU70Y8E"], "rxcui": ["857677", "857683"], "spl_set_id": ["0a95bc4f-34d3-4b5e-841b-6839e1c1e0c7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-939-00)", "package_ndc": "71205-939-00", "marketing_start_date": "20201119"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-939-30)", "package_ndc": "71205-939-30", "marketing_start_date": "20201119"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71205-939-55)", "package_ndc": "71205-939-55", "marketing_start_date": "20201119"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-939-60)", "package_ndc": "71205-939-60", "marketing_start_date": "20201119"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-939-90)", "package_ndc": "71205-939-90", "marketing_start_date": "20201119"}], "brand_name": "Terbutaline Sulfate", "product_id": "71205-939_9f8ee6b8-61e1-478a-90de-57358fdb5905", "dosage_form": "TABLET", "product_ndc": "71205-939", "generic_name": "Terbutaline Sulfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbutaline Sulfate", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "5 mg/1"}], "application_number": "ANDA211832", "marketing_category": "ANDA", "marketing_start_date": "20200713", "listing_expiration_date": "20261231"}