Triostat
- Product NDC
- 42023-120
- 11-digit product format
- 420230120
- Labeler code
- 42023
- Product ID
- 42023-120_480ffe8b-5e43-45bc-be8b-bc5731cfbe6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- liothyronine sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Par Pharmaceutical, Inc.
- Application
- NDA020105
- Marketing category
- NDA
- Marketing start
- 2013-05-01
- Marketing end
- 0000-00-00
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 10 ug/mL
- Pharmacologic classes
- l-Triiodothyronine [EPC],Triiodothyronine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42023-120-01 | 42023012001 | 1 VIAL, SINGLE-USE in 1 CARTON (42023-120-01) > 1 mL in 1 VIAL, SINGLE-USE | | 2013-05-01 | 0000-00-00 | No | No | Current |
| 42023-120-06 | 42023012006 | 6 VIAL in 1 CARTON (42023-120-06) > 1 mL in 1 VIAL | 6 vial | 2013-05-01 | 0000-00-00 | No | No | Current |