hyoscyamine sulfate
- Product NDC
- 71205-698
- Requested package NDC
- 71205-698-90
- 11-digit product format
- 712050698
- Labeler code
- 71205
- Product ID
- 71205-698_b027d9ba-34d3-4f52-b3a8-beb58b1c83d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hyoscyamine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-01-26
- Marketing end
- 0000-00-00
- Substance
- HYOSCYAMINE SULFATE
- Active strength
- 0 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 71205-698 | 71205-698-90 | D | Discontinued by firm | 2026-10-15 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71205-698-90 | 71205069890 | 90 TABLET in 1 BOTTLE (71205-698-90) | 90 tablet | 2022-09-16 | 0000-00-00 | No | No | Current |