NDC 16729-184 – Hydrochlorothiazide
Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC16729-184
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Accord Healthcare Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202556
- Marketed since
- April 10, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 50 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16729-184-01 | 100 TABLET in 1 BOTTLE (16729-184-01) | Apr 26, 2013 |
| 16729-184-17 | 1000 TABLET in 1 BOTTLE (16729-184-17) | Apr 10, 2013 |
Recalls mentioning this NDC
- D-1206-2018 Sep 19, 2018 · Class I
Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.
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