NDC 71205-868 – Ranolazine
Ranolazine 1000 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71205-868
Product details
- Brand name
- Ranolazine
- Generic name
- Ranolazine
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211829
- Marketed since
- August 24, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-anginal
Active ingredients
- Ranolazine 1000 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-868-00 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-00) | Dec 17, 2021 |
| 71205-868-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-30) | Dec 17, 2021 |
| 71205-868-55 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-55) | Dec 17, 2021 |
| 71205-868-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-60) | Dec 17, 2021 |
| 71205-868-72 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-72) | Dec 17, 2021 |
| 71205-868-78 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-78) | Dec 17, 2021 |
| 71205-868-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-90) | Dec 17, 2021 |
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