Levothyroxine
- Product NDC
- 43742-0955
- 11-digit product format
- 437420955
- Labeler code
- 43742
- Product ID
- 43742-0955_7c431149-4f46-4c4f-a5bb-c1b1fb705283
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Levothyroxine
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-01-06
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE
- Active strength
- 16 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43742-0955 | LEVOTHYROXINE LIQUID [DESERET BIOLOGICALS, INC.] | 3 | Legacy NDC | 20231214_1a467f8b-2611-4936-af2b-098e4791d6ae.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0955-1 | 43742095501 | 30 mL in 1 BOTTLE, DROPPER (43742-0955-1) | 30 ml | 2017-01-06 | 0000-00-00 | No | No | Current |