NDC 67877-218 – Metformin Hydrochloride
Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-218
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091184
- Marketed since
- January 31, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 850 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-218-01 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-218-01) | Jan 31, 2011 |
| 67877-218-05 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-218-05) | Jan 31, 2011 |
| 67877-218-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (67877-218-10) | Jan 31, 2011 |
| 67877-218-38 | 10 BLISTER PACK in 1 CARTON (67877-218-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-218-33) | Jan 31, 2011 |
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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