Losartan Potassium
- Product NDC
- 68180-211
- 11-digit product format
- 681800211
- Labeler code
- 68180
- Product ID
- 68180-211_38431fb6-7157-4be5-929a-0c65b7a29c55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA078232
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Losartan Potassium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOSARTAN POTASSIUM | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979480, 979485, 979492 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68180-211-01 | Losartan Potassium | 100 in 1 BOTTLE | TABLET | 100 | | 25 |
| 68180-211-03 | Losartan Potassium | 1000 in 1 BOTTLE | TABLET | 1000 | | 25 |
| 68180-211-06 | Losartan Potassium | 30 in 1 BOTTLE | TABLET | 30 | | 25 |
| 68180-211-09 | Losartan Potassium | 90 in 1 BOTTLE | TABLET | 90 | | 25 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| LOSARTAN POTASSIUM | ACTIVE INGREDIENT | 3ST302B24A | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| LOSARTAN | ACTIVE MOIETY | JMS50MPO89 | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| HYDROXYPROPYL CELLULOSE | INACTIVE INGREDIENT | RFW2ET671P | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 8 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-211 | LOSARTAN POTASSIUM TABLET [LUPIN PHARMACEUTICALS, INC.] | 22 | Current NDC, 4 package rows | 20240113_e5886220-43b7-46e1-9034-5242ba245bd1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68180-211-01 | 68180021101 | 100 in 1 BOTTLE | Historical |
| 68180-211-03 | 68180021103 | 1000 in 1 BOTTLE | Historical |
| 68180-211-06 | 68180021106 | 30 in 1 BOTTLE | Historical |
| 68180-211-09 | 68180021109 | 90 in 1 BOTTLE | Historical |