terbutaline sulfate

Generic: terbutaline sulfate

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name terbutaline sulfate
Generic Name terbutaline sulfate
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

terbutaline sulfate 5 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-133
Product ID 24979-133_3fd94b35-ef5a-4eb3-a3bd-0ce7572521d6
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 24979133
Hyphenated Format 24979-133

Supplemental Identifiers

RxCUI
857683 857677
UPC
0324979133010 0324979132013
UNII
576PU70Y8E

Packaging Origin

Original Packager
true

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 (24979-133-01)
  • 1000 TABLET in 1 BOTTLE (24979-133-03)
source: ndc

Packages (2)

24979-133-01 100 TABLET in 1 BOTTLE (24979-133-01) 24979-133-03 1000 TABLET in 1 BOTTLE (24979-133-03)

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": "3fd94b35-ef5a-4eb3-a3bd-0ce7572521d6", "openfda": {"upc": ["0324979133010", "0324979132013"], "unii": ["576PU70Y8E"], "rxcui": ["857683", "857677"], "spl_set_id": ["3a4e5046-293c-4616-8679-6da65f31626b"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (24979-133-01)", "package_ndc": "24979-133-01", "marketing_start_date": "20200713"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (24979-133-03)", "package_ndc": "24979-133-03", "marketing_start_date": "20200713"}], "brand_name": "Terbutaline Sulfate", "product_id": "24979-133_3fd94b35-ef5a-4eb3-a3bd-0ce7572521d6", "dosage_form": "TABLET", "product_ndc": "24979-133", "generic_name": "Terbutaline Sulfate", "labeler_name": "Upsher-Smith Laboratories, LLC", "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"}