Clobetasol Propionate
- Product NDC
- 71205-151
- 11-digit product format
- 712050151
- Labeler code
- 71205
- Product ID
- 71205-151_4d97dda6-6c71-4595-9871-fc85c8e4f73b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA074139
- Marketing category
- ANDA
- Marketing start
- 2014-02-03
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-151 | CLOBETASOL PROPIONATE CREAM [PROFICIENT RX LP] | 3 | Legacy NDC | 20191115_3ff0b387-b83a-4e5a-b9c0-faa33b319a3c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-151-15 | 71205015115 | 1 TUBE in 1 CARTON (71205-151-15) > 15 g in 1 TUBE | 1 tube | 2018-11-01 | 0000-00-00 | No | No | Current |