ANZEMET
- Product NDC
- 30698-220
- 11-digit product format
- 306980220
- Labeler code
- 30698
- Product ID
- 30698-220_3b3a8574-591c-46b7-99cc-adca27a22c01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dolasetron mesylate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Validus Pharmaceuticals LLC
- Application
- NDA020623
- Marketing category
- NDA
- Marketing start
- 1997-09-11
- Marketing end
- 0000-00-00
- Substance
- DOLASETRON MESYLATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 30698-220-10 | ANZEMET | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30698-220 | ANZEMET (DOLASETRON MESYLATE) TABLET, FILM COATED [VALIDUS PHARMACEUTICALS LLC] | 6 | Legacy NDC, 1 package rows | 20231215_201b0eb8-4a1e-4e22-ab4b-addb642710d6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30698-220-10 | 30698022010 | 10 TABLET, FILM COATED in 1 BOTTLE (30698-220-10) | 1997-09-11 | 0000-00-00 | No | No | Current |