Terbutaline Sulfate
- Product NDC
- 71872-7080
- 11-digit product format
- 718727080
- Labeler code
- 71872
- Product ID
- 71872-7080_fc5fc617-c901-4ee6-e053-6294a90aeb43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbutaline Sulfate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Medical Purchasing Solutions. LLC
- Application
- ANDA078630
- Marketing category
- ANDA
- Marketing start
- 2009-05-20
- Substance
- TERBUTALINE SULFATE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Terbutaline Sulfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TERBUTALINE SULFATE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 576PU70Y8E |
| Rxcui | 857635 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7080-1 | Terbutaline Sulfate | 1 mL in 1 VIAL | INJECTION | 1 | | 4 |
| 71872-7080-1 | Terbutaline Sulfate | 1 in 1 BAG | INJECTION | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71872-7080 | TERBUTALINE SULFATE INJECTION [MEDICAL PURCHASING SOLUTIONS. LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20230524_6a22b62c-4ee1-49df-e053-2a91aa0a3e52.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7080-1 | 71872708001 | 1 VIAL in 1 BAG (71872-7080-1) / 1 mL in 1 VIAL | 1 vial | 2018-03-06 | 0000-00-00 | No | No | Current |