GRANISETRON HYDROCHLORIDE
- Product NDC
- 69097-197
- 11-digit product format
- 690970197
- Labeler code
- 69097
- Product ID
- 69097-197_d8067707-a4ff-416d-98f3-b65ad6610f71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GRANISETRON HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Cipla USA Inc.
- Application
- ANDA078258
- Marketing category
- ANDA
- Marketing start
- 2008-06-30
- Marketing end
- 0000-00-00
- Substance
- GRANISETRON HYDROCHLORIDE
- Active strength
- 4 mg/4mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#