Qualaquin
- Product NDC
- 49708-153
- 11-digit product format
- 497080153
- Labeler code
- 49708
- Product ID
- 49708-153_ec714122-b9cd-45c8-b39a-dea83b1eb2aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinine Sulfate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- NDA021799
- Marketing category
- NDA
- Marketing start
- 2005-08-12
- Marketing end
- 0000-00-00
- Substance
- QUININE SULFATE
- Active strength
- 324 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 49708-153-07 | 49708015307 | 30 CAPSULE in 1 BOTTLE, PLASTIC (49708-153-07) | 30 capsule | 2005-08-12 | 0000-00-00 | No | No | Current |