Clotrimazole
- Product NDC
- 70518-2932
- 11-digit product format
- 705182932
- Labeler code
- 70518
- Product ID
- 70518-2932_dd161290-b587-792e-e053-2a95a90a57ca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clotrimazole
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072641
- Marketing category
- ANDA
- Marketing start
- 2020-11-04
- Marketing end
- 0000-00-00
- Substance
- CLOTRIMAZOLE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2932-0 | 70518293200 | 1 TUBE in 1 CARTON (70518-2932-0) > 45 g in 1 TUBE | 1 tube | 2020-11-04 | 0000-00-00 | No | No | Current |