Telmisartan and Amlodipine
- Product NDC
- 68180-198
- 11-digit product format
- 681800198
- Labeler code
- 68180
- Product ID
- 68180-198_db056024-a5b4-4f2a-8fe0-8ee308cf5700
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan and Amlodipine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA201586
- Marketing category
- ANDA
- Marketing start
- 2014-01-08
- Marketing end
- 0000-00-00
- Substance
- TELMISARTAN; AMLODIPINE BESYLATE
- Active strength
- 80 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68180-198-06 | Telmisartan and Amlodipine | 30 in 1 BOTTLE | TABLET | 30 | | 10 |
| 68180-198-09 | Telmisartan and Amlodipine | 90 in 1 BOTTLE | TABLET | 90 | | 10 |
| 68180-198-12 | Telmisartan and Amlodipine | 10 in 1 BLISTER PACK | TABLET | 10 | | 10 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| AMLODIPINE BESYLATE | ACTIVE INGREDIENT | 864V2Q084H | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| TELMISARTAN | ACTIVE INGREDIENT | U5SYW473RQ | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| AMLODIPINE | ACTIVE MOIETY | 1J444QC288 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| TELMISARTAN | ACTIVE MOIETY | U5SYW473RQ | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-198 | TELMISARTAN AND AMLODIPINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 10 | Legacy NDC, 3 package rows | 20231216_a97fefa6-99e6-4eb7-9393-ab2252a2c7d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-198-06 | 68180019806 | 30 TABLET in 1 BOTTLE (68180-198-06) | 30 tablet | 2014-01-08 | 0000-00-00 | No | No | Current |
| 68180-198-09 | 68180019809 | 90 TABLET in 1 BOTTLE (68180-198-09) | 90 tablet | 2014-01-08 | 0000-00-00 | No | No | Current |
| 68180-198-12 | 68180019812 | 10 TABLET in 1 BLISTER PACK (68180-198-12) | 10 tablet | 2014-01-08 | 0000-00-00 | No | No | Current |