Losortan Potassium
- Product NDC
- 63739-673
- 11-digit product format
- 637390673
- Labeler code
- 63739
- Product ID
- 63739-673_e2ad6eff-97fc-135a-e053-2a95a90afed5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mckesson Corporation DBA SKY Packaginng
- Application
- ANDA078243
- Marketing category
- ANDA
- Marketing start
- 2010-10-04
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-673 | LOSARTAN POTASSIUM TABLET, FILM COATED LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [MCKESSON CORPORATION DBA SKY PACKAGINNG] | 15 | Legacy NDC | 20241228_8c98555b-2931-4e6b-b155-1e6525cb263d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-673-10 | 63739067310 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-673-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2016-10-19 | 0000-00-00 | No | No | Current |