Terbutaline Sulfate
- Product NDC
- 10271-101
- 11-digit product format
- 102710101
- Labeler code
- 10271
- Product ID
- 10271-101_2a4be57a-a3df-4aa5-be52-845b75e78b3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbutaline Sulfate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- United Biomedical Inc., Asia
- Application
- ANDA200122
- Marketing category
- ANDA
- Marketing start
- 2014-12-15
- Marketing end
- 0000-00-00
- Substance
- TERBUTALINE SULFATE
- Active strength
- 1 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10271-101-10 | Terbutaline Sulfate | 1 mL in 1 VIAL | INJECTION | 1 | | 1 |
| 10271-101-10 | Terbutaline Sulfate | 10 in 1 BOX | INJECTION | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10271-101 | TERBUTALINE SULFATE INJECTION [UNITED BIOMEDICAL INC., ASIA] | 1 | Legacy NDC, 2 package rows | 20141215_2a4be57a-a3df-4aa5-be52-845b75e78b3b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 10271-101-10 | 10271010110 | 1 mL in 1 VIAL | 1 ml | Historical |