Clindamycin Hydrochloride
- Product NDC
- 0527-1381
- 11-digit product format
- 005271381
- Labeler code
- 0527
- Product ID
- 0527-1381_cc80896e-4a77-45d4-8625-9ac72e5fbfd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA065243
- Marketing category
- ANDA
- Marketing start
- 2005-08-12
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE]
- 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 |
|---|
| 0527-1381-01 | 00527138101 | 100 CAPSULE in 1 BOTTLE (0527-1381-01) | 100 capsule | 2005-08-12 | 0000-00-00 | No | No | Current |
| 0527-1381-04 | 00527138104 | 200 CAPSULE in 1 BOTTLE (0527-1381-04) | 200 capsule | 2005-08-12 | 0000-00-00 | No | No | Current |