NDC 68682-021 – Metformin hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68682-021
Product details
- Brand name
- Metformin hydrochloride
- Generic name
- metformin hydrochloride
- Labeler
- Oceanside Pharmaceuticals
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021748
- Marketed since
- March 20, 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 68682-021-50 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-021-50) | Mar 20, 2018 |
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