Clindamycin Hydrochloride
- Product NDC
- 68071-3175
- 11-digit product format
- 680713175
- Labeler code
- 68071
- Product ID
- 68071-3175_bbf110a2-292f-2ed9-e053-2a95a90a52b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA063083
- Marketing category
- ANDA
- Marketing start
- 1991-07-31
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3175-4 | 68071317504 | 4 CAPSULE in 1 BOTTLE (68071-3175-4) | 4 capsule | 2017-03-17 | 0000-00-00 | No | No | Current |
| 68071-3175-6 | 68071317506 | 6 CAPSULE in 1 BOTTLE (68071-3175-6) | 6 capsule | 2017-03-17 | 0000-00-00 | No | No | Current |