GRANISETRON HYDROCHLORIDE
- Product NDC
- 69097-195
- 11-digit product format
- 690970195
- Labeler code
- 69097
- Product ID
- 69097-195_041ba64c-c295-46b9-a27b-5d584b55ba8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GRANISETRON HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Cipla USA Inc.
- Application
- ANDA078262
- Marketing category
- ANDA
- Marketing start
- 2007-12-31
- Marketing end
- 0000-00-00
- Substance
- GRANISETRON HYDROCHLORIDE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record