NDC 67877-413 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral
Product NDC67877-413
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206145
- Marketed since
- October 27, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 67877-413-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-413-01) | Oct 27, 2018 |
| 67877-413-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-413-05) | Oct 27, 2018 |
| 67877-413-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-413-10) | Oct 27, 2018 |
| 67877-413-33 | 10 BLISTER PACK in 1 CARTON (67877-413-33) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Oct 27, 2018 |
| 67877-413-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-413-90) | Dec 27, 2019 |
Recalls mentioning this NDC
- D-0163-2017 Dec 7, 2016 · Class II
Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP
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