UNITHROID
- Product NDC
- 0527-1639
- 11-digit product format
- 005271639
- Labeler code
- 0527
- Product ID
- 0527-1639_22c86d10-1b7b-448f-8004-1191fea738fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- NDA021210
- Marketing category
- NDA
- Marketing start
- 2007-10-01
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 0 mg/1
- Pharmacologic classes
- l-Thyroxine [EPC],Thyroxine [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 |
|---|
| 0527-1639-01 | 00527163901 | 100 TABLET in 1 BOTTLE, PLASTIC (0527-1639-01) | 100 tablet | 2007-10-01 | 0000-00-00 | No | No | Current |