NDC 62756-142 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral
Product NDC62756-142
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077336
- Marketed since
- February 9, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62756-142-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01) | Feb 9, 2006 |
| 62756-142-02 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02) | Feb 9, 2006 |
Recalls mentioning this NDC
- D-0372-2021 May 19, 2021 · Class II
Presence of foreign substance: identified as activated carbon. - D-0325-2021 Apr 14, 2021 · Class III
Failed Moisture Limits: Out of specification for water content - D-0924-2018 Jul 25, 2018 · Class II
Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one… - D-1089-2014 Mar 5, 2014 · Class II
Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin found in a bottle of Metformin HCl ER
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