terbutaline sulfate

Generic: terbutaline sulfate

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name terbutaline sulfate
Generic Name terbutaline sulfate
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

terbutaline sulfate 2.5 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-721
Product ID 62559-721_ee722f8c-05d6-43bc-825d-9496579032c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA017849
Listing Expiration 2026-12-31
Marketing Start 2018-10-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559721
Hyphenated Format 62559-721

Supplemental Identifiers

RxCUI
857677 857683
UPC
0362559721011 0362559722018
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 NDA017849 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (62559-721-01)
source: ndc

Packages (1)

62559-721-01 100 TABLET in 1 BOTTLE (62559-721-01)

Ingredients (1)

terbutaline sulfate (2.5 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": "ee722f8c-05d6-43bc-825d-9496579032c4", "openfda": {"upc": ["0362559721011", "0362559722018"], "unii": ["576PU70Y8E"], "rxcui": ["857677", "857683"], "spl_set_id": ["d810a15b-3e10-4f6c-a36e-8ddecbaba9c3"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-721-01)", "package_ndc": "62559-721-01", "marketing_start_date": "20181016"}], "brand_name": "Terbutaline Sulfate", "product_id": "62559-721_ee722f8c-05d6-43bc-825d-9496579032c4", "dosage_form": "TABLET", "product_ndc": "62559-721", "generic_name": "Terbutaline Sulfate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbutaline Sulfate", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "2.5 mg/1"}], "application_number": "NDA017849", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20181016", "listing_expiration_date": "20261231"}