Terbutaline Sulfate

Product NDC
70860-801
11-digit product format
708600801
Labeler code
70860
Product ID
70860-801_298ff47f-dea9-473f-ba9b-ca1427d4dcb4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
terbutaline sulfate
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Labeler
Athenex Pharmaceutical Division, LLC.
Application
ANDA200122
Marketing category
ANDA
Marketing start
2017-02-22
Marketing end
0000-00-00
Substance
TERBUTALINE SULFATE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
49ccb555-d142-0761-ee45-2e1304b37b1dProduct name220210111
a3c04a67-87ea-e8b8-0458-db8085ac6340Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70860-801-01ML - Milliliter70860-80115744f61-7836-49ea-8d79-12c02131e36112017-07-07
70860-801-41ML - Milliliter70860-8011822aea5-1e72-4fbe-bf54-ecbd36b7ffe312019-05-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
857635terbutaline sulfate 1 MG in 1 ML InjectionPSN69488fbd-0193-570f-e053-2991aa0af0ed2
8576351 ML terbutaline sulfate 1 MG/ML InjectionSCD69488fbd-0193-570f-e053-2991aa0af0ed2
857635terbutaline sulfate 1 MG per 1 ML InjectionSY69488fbd-0193-570f-e053-2991aa0af0ed2