Clindamycin hydrochloride
- Product NDC
- 70518-4583
- 11-digit product format
- 705184583
- Labeler code
- 70518
- Product ID
- 70518-4583_5268de18-65de-4253-e063-6394a90a6d4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065061
- Marketing category
- ANDA
- Marketing start
- 2026-03-09
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Clindamycin hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLINDAMYCIN HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | T20OQ1YN1W |
| Rxcui | 197518 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4583-0 | Clindamycin hydrochloride | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4583-0 | 70518458300 | 30 CAPSULE in 1 BLISTER PACK (70518-4583-0) | 30 capsule | 2026-03-09 | No | No | Current |