CLINDAMYCIN HYDROCHLORIDE
- Product NDC
- 71335-2677
- 11-digit product format
- 713352677
- Labeler code
- 71335
- Product ID
- 71335-2677_4809266d-d1f1-46b1-b268-5c943ad5ecf1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207402
- Marketing category
- ANDA
- Marketing start
- 2019-01-07
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| T20OQ1YN1W | CLINDAMYCIN HYDROCHLORIDE | 21462-39-5 | CLINDAMYCIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2677-1 | 71335267701 | 10 CAPSULE in 1 BOTTLE (71335-2677-1) | 10 capsule | 2025-09-11 | No | No | Historical |