NDC 68462-840 – Telmisartan and Hydrochlorothiazide
Telmisartan 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC68462-840
Product details
- Brand name
- Telmisartan and Hydrochlorothiazide
- Generic name
- Telmisartan and Hydrochlorothiazide
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202544
- Marketed since
- March 4, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Telmisartan 40 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Telmisartan And Hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68462-840-13 | 3 BLISTER PACK in 1 CARTON (68462-840-13) / 10 TABLET in 1 BLISTER PACK | Mar 4, 2019 |
Recalls mentioning this NDC
- D-1306-2022 Aug 17, 2022 · Class II
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister . - D-1305-2022 Aug 17, 2022 · Class II
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
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