NDC 52389-155 – Diurex Ultra
Caffeine 100 mg/1 · Tablet, Film Coated · Oral
Product NDC52389-155
Product details
- Brand name
- Diurex Ultra
- Generic name
- Caffeine
- Labeler
- Kobayashi Healthcare International, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M027
- Marketed since
- September 1, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant; Methylxanthine
Active ingredients
- Caffeine 100 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 52389-155-02 | 2 BOTTLE, PLASTIC in 1 PACKAGE (52389-155-02) / 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | Jan 4, 2024 |
| 52389-155-80 | 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-155-80) | Sep 1, 2005 |
| 52389-155-90 | 1 BOTTLE in 1 CARTON (52389-155-90) / 90 TABLET, FILM COATED in 1 BOTTLE | Sep 1, 2005 |
Other Diurex products
- 52389-249 Pamabrom 50 mg/1 · Tablet, Film Coated · Kobayashi Healthcare International, Inc.
- 52389-656 Caffeine 100 mg/1 · Tablet, Film Coated · Kobayashi Healthcare International, Inc.
- 52389-306 Magnesium Salicylate 162.5 mg/1; Caffeine 50 mg/1 · Tablet, Coated · Kobayashi Healthcare International, Inc.