Quinine Sulfate
- Product NDC
- 53489-700
- 11-digit product format
- 534890700
- Labeler code
- 53489
- Product ID
- 53489-700_d18ebeb2-8589-423b-8c0d-4b6a11b64443
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinine Sulfate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- NDA021799
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-07-23
- Marketing end
- 0000-00-00
- Substance
- QUININE SULFATE
- Active strength
- 324 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 53489-700-01 | 53489070001 | 100 CAPSULE in 1 BOTTLE, PLASTIC (53489-700-01) | 100 capsule | 2012-07-23 | 0000-00-00 | No | No | Current |
| 53489-700-07 | 53489070007 | 30 CAPSULE in 1 BOTTLE, PLASTIC (53489-700-07) | 30 capsule | 2012-07-23 | 0000-00-00 | No | No | Current |