Bisacodyl
- Product NDC
- 55700-502
- 11-digit product format
- 557000502
- Labeler code
- 55700
- Product ID
- 55700-502_f6ca0d63-6ef3-461a-887b-ff98e03d9c58
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- bisacodyl
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-02-10
- Marketing end
- 0000-00-00
- Substance
- BISACODYL
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record