NDC 70069-848 – Rilpivirine
Rilpivirine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC70069-848
Product details
- Brand name
- Rilpivirine
- Generic name
- Rilpivirine
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA218798
- Marketed since
- January 30, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor
Active ingredients
- Rilpivirine Hydrochloride 25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70069-848-30 | 30 TABLET, FILM COATED in 1 BOTTLE (70069-848-30) | Jan 30, 2026 |
Other Rilpivirine products
- 42385-999 Rilpivirine Hydrochloride 25 mg/1 · Tablet, Film Coated · Laurus Labs Limited