Donnatal
- Product NDC
- 42291-245
- 11-digit product format
- 422910245
- Labeler code
- 42291
- Product ID
- 42291-245_d57a0a79-c3c6-3000-e053-2995a90a7c25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2014-01-06
- Marketing end
- 0000-00-00
- Substance
- PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE
- Active strength
- 16 mg/1; mg/1; mg/1; mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 42291-245-01 | 42291024501 | 100 TABLET in 1 BOTTLE (42291-245-01) | 100 tablet | 2014-01-06 | 0000-00-00 | No | No | Current |