NDC 72789-561 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-561
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213320
- Marketed since
- August 25, 2025
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 72789-561-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-20) | Apr 14, 2026 |
| 72789-561-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-30) | Apr 29, 2026 |
| 72789-561-42 | 42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-42) | Aug 4, 2026 |
| 72789-561-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-60) | Apr 16, 2026 |
| 72789-561-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-90) | May 27, 2026 |
| 72789-561-93 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-93) | Apr 16, 2026 |
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