NDC 0054-8301 – Furosemide
Furosemide 80 mg/1 · Tablet · Oral
Product NDC0054-8301
Product details
- Brand name
- Furosemide
- Generic name
- Furosemide
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA070086
- Marketed since
- March 13, 1991
- Listing expires
- December 31, 2027
- Pharmacologic class
- Loop Diuretic
Active ingredients
- Furosemide 80 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0054-8301-25 | 10 BLISTER PACK in 1 CARTON (0054-8301-25) / 10 TABLET in 1 BLISTER PACK | Mar 13, 1991 |
Recalls mentioning this NDC
- D-0437-2017 Feb 1, 2017 · Class II
Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint. - D-0011-2016 Oct 21, 2015 · Class III
CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP. - D-0012-2016 Oct 21, 2015 · Class III
CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.
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